Sunday, November 29, 2015

New #drug #recall of Glades multivitamin containing high amounts of Vitamin D3.

FDA Announces Glades Drugs' Nationwide Voluntary Recall Of Compounded Multivitamins Containing High Amounts Of Vitamin D3 (Cholecalciferol)

Contact: Faith Washington, Pharmacist
 (866) 597-3296

The U.S. Food and Drug Administration is alerting health care professionals and patients of a voluntary recall of compounded multivitamin capsules containing high amounts of Vitamin D3 (Cholecalciferol), distributed nationwide by Glades Drugs in Pahokee, Florida. FDA has received reports of several adverse events potentially associated with these compounded capsules made by Glades Drugs.

Consumption of this product may result in vitamin D toxicity, which may be severe and may lead to life-threatening outcomes if left untreated. Patients suffering adverse effects from high Vitamin D levels (Cholecalciferol) may not initially show symptoms. Therefore, patients who have received these compounded capsules should stop taking this medication and immediately seek medical attention.

Symptoms of short-term vitamin D toxicity are due to high calcium levels (also known as hypercalcemia) and include confusion, increased urination, increased thirst, loss of appetite, vomiting, and muscle weakness. Acute hypercalcemia may intensify tendencies for heart arrhythmias and seizures and may increase the effects of certain heart drugs. Long-term toxicity may cause kidney failure, increase in calcium deposits in the blood and soft tissue, bone demineralization and pain. Patients with conditions such as liver disease or chronic kidney failure may be at increased risk for developing vitamin D toxicity.

Health care providers should quarantine and return any products subject to this recall to the company at: Glades Drugs, 109 S. Lake Ave., Pahokee, FL 33476. Glades Drugs sent recall letters to patients, attempted to contact them by phone, and called prescribing physicians.

FDA encourages health care professionals and patients to report adverse reactions to theFDA’s MedWatch Adverse Event Reporting program:

Complete and submit the report online atwww.fda.gov/medwatch/report.htm; orDownload and complete the form, then submit it via fax at 1-800-FDA-0178.

Friday, November 27, 2015

New #foodsafety #recall of Mama Lina’s Inc. Beef and Chicken Empanada Products Produced Without Benefit of Inspection

Mama Lina’s Inc. Recalls Beef and Chicken Empanada Products Produced Without Benefit of Inspection

Class I Recall

144-2015

Health Risk: High

Nov 27, 2015

Congressional and Public Affairs
Brittany C. Woodland
(202) 720-9113

WASHINGTON, Nov. 27, 2015 – Mama Lina’s Inc., a San Diego, Calif. establishment, is recalling approximately 1,754 pounds of beef and chicken empanada products that were produced without the benefit of federal inspection, the U.S. Department of Agriculture’s Food Safety and Inspection Service (FSIS) announced today.

The beef, chicken, sweet wine beef and chipotle chicken empanada items were produced on August 31, 2015 and September 29, 2015. The following products are subject to recall: [View Labels (PDF Only)]

330- lb. (approximately) cases and bags containing pieces of “CHIPOTLE CHICKEN EMPANADA.”322.13-lb. (approximately) cases, trays and bags containing pieces of “BEEF EMPANADA.”1095-lb. (approximately) cases, trays and bags containing pieces of “CHICKEN EMPANADA.”7.13-lb. (approximately) bag containing pieces of “SWEET WINE BEEF EMPANADA.”

The products subject to recall bear establishment number “EST. 2012” inside the USDA mark of inspection. These items were shipped to a retail location San Diego, CA.

The problem was discovered during routine FSIS inspection. The beef empanadas and chicken empanadas were found in the establishment’s freezer and did not have the marks of FSIS inspection. The products had a “deli” sticker and labels indicating that the products are manufactured by another entity, which leases part of the facility from Mama Lina’s.

There have been no confirmed reports of adverse reactions due to consumption of these products. Anyone concerned about a reaction should contact a healthcare provider.

Consumers who have purchased these products are urged not to consume them. These products should be thrown away or returned to the place of purchase.

FSIS routinely conducts recall effectiveness checks to verify recalling firms notify their customers of the recall and that steps are taken to make certain that the product is no longer available to consumers. When available, the retail distribution list(s) will be posted on the FSIS website at www.fsis.usda.gov/recalls.

Consumers or Media with questions about the recall can contact Alma Villarruel, Mama Lina’s Inc., Office Manager, at (858) 535-0620.

Consumers with food safety questions can "Ask Karen," the FSIS virtual representative available 24 hours a day atAskKaren.gov or via smartphone at m.askkaren.gov. The toll-free USDA Meat and Poultry Hotline 1-888-MPHotline (1-888-674-6854) is available in English and Spanish and can be reached from l0 a.m. to 4 p.m. (Eastern Time) Monday through Friday. Recorded food safety messages are available 24 hours a day. The online Electronic Consumer Complaint Monitoring System can be accessed 24 hours a day at:http://www.fsis.usda.gov/reportproblem.

USDA Recall ClassificationsClass IThis is a health hazard situation where there is a reasonable probability that the use of the product will cause serious, adverse health consequences or death.Class IIThis is a health hazard situation where there is a remote probability of adverse health consequences from the use of the product.Class IIIThis is a situation where the use of the product will not cause adverse health consequences.

Thursday, November 26, 2015

New #foodsafety #recall possible #ecoli contamination of products containing #celery

Taylor Farms Pacific, Inc. Recalls Celery Products Because Of Possible Health Risk

Contact: Taylor Farms Pacific, Inc.
 (209) 830-3141

Taylor Farms Pacific, Inc. of Tracy, CA, is recalling the products listed below because they may include celery which could potentially contain E. coli 0157:H7. The products listed below are being recalled out of an abundance of caution due to a Celery and Onion Diced Blend testing positive for E. coli0157:H7 in a sample taken by the Montana Department of Health. The Celery and Onion Diced Blend tested by the state of Montana was used in a Costco Rotisserie Chicken Salad that has been linked to a multi-state E. coli 0157:H7 outbreak.

Escherichia coli O157:H7 is a bacterium that causes a diarrheal illness often with bloody stools. Although most healthy adults can recover completely within a week, some people can develop a form of kidney failure called Hemolytic Uremic Syndrome (HUS). HUS is most likely to occur in young children and the elderly. The condition can lead to serious kidney damage and even death.

Internal Item CodeProductDescription of PackagingStoreLot CodesQuantityUse By DateStores Distributed271820Fresh To Go Bistro Snack 1/7.5oz Tray $4.29Tray7-ElevenTF 317, 319, 320, 321, 322, 324, 326, 327, 328280811/20/15 to 12/1/15Ca., Nv., Wa., Or., Co240088CST Celery 1/4" Dice 8/5# BagFood Service BagCostcoTF 317, 319, 320, 321, 322, 32310411/20/15 to 12/8/15Ca., Az., Nv., Ut., Wa.240069CST Celery Dcd 1/4" 2/5# BagFood Service BagCostcoTF 313, 314, 316, 317, 319, 320, 321, 324, 326, 3272911/20/15 to 12/8/15Ca., Wa., Or., Id.240028CST Celery Sticks 4" 8/5# BagFood Service BagCostcoTF 313, 314, 315, 316, 317, 319, 320, 321, 323, 324, 326, 327, 32822911/20/15 to 12/8/15Ca., Az., Nv., Ut., Wa., Il., Ga.240063CST Celery/Onion 1/4" Dcd Blend 3/4# BagFood Service BagCostcoTF 313, 314, 315, 316, 317, 319, 320, 321, 322, 323118411/20/15 to 12/8/15Ca., Wa., Or., Id., Mt., Ut., Co.202040CST Turkey Dinner Veggie 6/12oz BagFood Service BagCostcoTF 319, 320, 321, 322, 323, 324217011/20/15 to 12/8/15Ca., Wa., Or., Id., Mt., Ut., Co.202241TF Chicken Salad W/ Grapes 2Cnt Salad KitBulk KitKing SooperTF 313, 314, 315, 317, 320, 321, 322, 324, 328110611/20/15 to 12/8/15Co., Wy.203022TF Curry Chicken 2Cnt Salad KitBulk KitKing SooperTF 313, 314, 315, 317, 318, 320, 321, 322, 324, 32812711/20/15 to 12/8/15Co., Wy.202139TF-KS Apple Waldorf 2Cnt Salad KitBulk KitKing SooperTF 313, 314, 315, 317, 320, 32843411/20/15 to 12/8/15Co., Wy.278902Citizen Chef Pantry Buffalo Chicken Wrap 1/10oz TrayTrayPantryTF 320, 321, 326, 327, 328, 32912911/20/15 to 11/30/15Ca.278003Citizen Chef Pantry Asian W/Chckn Premade Salad 10.25oz TrayPremade SaladPantryTF 319, 320, 321, 322, 326, 327, 32812611/20/15 to 12/1/15Ca.201428Raley's Albacore Tuna Salad Kit - 0595143Bulk KitRaleysTF 315, 316, 317, 318, 320, 322, 324, 325, 32729011/20/15 to 12/6/15Ca ,Nv.270280Raley's Asian Pasta Toss 1/12oz TrayPremade SaladRaleysTF 313, 314, 316, 318, 319, 320, 322, 324, 326, 327, 328174811/20/15 to 12/4/15Ca.,Nv.201426Raley's Blue Cheese Potato&Bacon Salad - 0595129Bulk KitRaleysTF 314, 315, 316, 318, 320, 324, 325, 327, 32838011/20/15 to 12/5/15Ca.,Nv.210397Raley's Buffalo Roasted Cauliflower KitBulk KitRaleysTF 313, 314, 315, 317, 318, 320, 321, 324, 325, 3269011/20/15 to 12/6/15Ca.,Nv.271973Raley's Country Potato Salad 1/32oz TrayTrayRaleysTF 317, 319, 321, 322, 323, 324, 326, 327, 328300611/20/15 to 12/4/15Ca.,Nv.271970Raley's Country Macaroni Salad 1/16oz TrayTrayRaleysTF 317, 319, 321, 323, 324, 326, 327, 32878411/20/15 to 12/4/15Ca.,Nv.271971Raley's Country Macaroni Salad 1/32oz TrayTrayRaleysTF 317, 319, 321, 322, 323, 324, 326, 327, 328224811/20/15 to 12/4/15Ca.,Nv.271972Raley's Country Potato Salad 1/16oz TrayTrayRaleysTF 317, 319, 321, 322, 323, 324, 326, 327, 328327811/20/15 to 12/4/15Ca.,Nv.201675Raley's Crunchy Veggie Salad KitBulk KitRaleysTF 313, 314, 315, 316, 317, 318, 320, 321, 322, 324, 325, 327, 328200511/20/15 to 12/6/15Ca.,Nv.210392Raley's Curry Chicken Salad KitBulk KitRaleysTF 313, 314, 315, 317, 318, 320, 322, 324, 325, 326, 32856511/20/15 to 12/6/15Ca.,Nv.201508Raley's Golden State Chicken Salad KitBulk KitRaleysTF 313, 314, 315, 316, 317, 318, 320, 322, 324, 325, 32799211/20/15 to 12/6/15Ca.,Nv.201674Raley's Loaded Potato Salad KitBulk KitRaleysTF 313, 314, 315, 316, 317, 318, 320, 321, 322, 324, 325, 327, 328121811/20/15 to 12/6/15Ca.,Nv.201427Raley's Mandarin Orange Chinese W/Chicken KitBulk KitRaleysTF 313, 314, 315, 317, 318, 320, 321, 324, 325, 326, 327, 32863011/20/15 to 12/6/15Ca.,Nv.201412Raley's Nob Hill Recovery Chicken Salad KitBulk KitRaleysTF 315, 317, 318, 320, 321, 322, 324, 325, 3277011/20/15 to 12/6/15Ca.,Nv.201480Raley's Old Fashion Salad W/Chicken - 0595254Bulk KitRaleysTF 313, 314, 316, 317, 318, 320, 324, 325, 327103111/20/15 to 12/6/15Ca.,Nv.201433Raley's Seafood Salad - 0595077Bulk KitRaleysTF 313, 314, 315, 316, 317, 318, 320, 322, 324, 325, 327, 328226011/20/15 to 12/6/15Ca.,Nv.201359Raley's Thanksgiving Salad KitBulk KitRaleysTF 313, 314, 315, 317, 318, 320, 321, 322, 324, 325, 32757011/20/15 to 12/6/15Ca.,Nv.271752Raley's Traditional Cornbread Stuffing 25oz TrayTrayRaleysTF 321, 322, 3231255811/20/15 to 12/1/15Ca.,Nv.271727Raley's Vegetable 1/3# TrayTrayRaleysTF 315, 316, 317, 319, 320, 321, 323, 324, 326, 327, 329221811/20/15 to 12/6/15Ca.,Nv.271758Raley's Vegetable and Ranch Dip 1/27oz TrayTrayRaleysTF 315, 316, 319, 320, 321, 322, 323, 324, 326, 32793111/20/15 to 12/6/15Ca.,Nv.270352Savemart/FM/Lucky Buffalo Style Chicken Wrap 1/10ozSandwich WrapSavemartTF 319, 320, 321, 322, 323, 32760311/20/15 to 11/30/15Ca.270359Savemart/FM/Lucky Fully Loaded Chopped Salad 1/10.5oz TrayPremade SaladSavemartTF 317, 319, 320, 321, 322, 323, 324, 32737711/20/15 to 12/1/15Ca.270366Savemart/FM/Lucky Greek Salad 1/10.5oz TrayPremade SaladSavemartTF 317, 319, 320, 321, 322, 323, 324, 32738611/20/15 to 12/1/15Ca.270363Savemart/FM/Lucky Southwest W/ Chicken Salad 1/9.5oz TrayPremade SaladSavemartTF 317, 319, 320, 321, 322, 323, 32757611/20/15 to 12/1/15Ca.200524TF Sicilian Vegetable Salad 2Ct KitBulk KitSavemartTF 313, 314, 315, 316, 317, 319, 320, 322, 323, 3275311/20/15 to 12/8/15Ca210160TF Asian Chopped Round Toss Up Salad 6/6oz TrayPremade SaladSavemart/ Tonys/ AlbertsonsTF 316, 317, 319, 320, 323, 32770011/20/15 to 12/8/15Ca.279003Sig Cafe Asian W/Chicken Premade Salad 10.25oz TrayPremade SaladSafeway / AlbertsonsTF 317, 321, 322, 323, 324, 325, 326, 327, 3281122211/20/15 to 12/1/15Ca., Nv., Or., Az., Nm., Wy., Sd., Ne.203326TF Crunchy Vegetables 2ct Salad KitBulk KitAlbertsonsTF 314, 316, 317, 320, 321, 32715511/20/15 to 12/8/15Or.218858Sig Cafe Asian W/Chicken Premade Salad 4/10.25oz TrayPremade SaladAlbertsonsTF 317, 319, 320, 321, 322, 323, 324, 326, 327, 32857911/20/15 to 12/1/15Ca.218871Sig Cafe Thai Style W/ Chicken Premade Salad 4/12oz TrayPremade SaladAlbertsonsTF 317, 319, 320, 321, 322, 323, 324, 326, 327, 32853911/20/15 to 12/1/15Ca.203017TF Cheesy Bacon Ranch Pasta 2Cnt SaladBulk KitAlbertsonsTF 314, 315, 316, 317, 320, 321, 322, 324, 325, 326, 32753511/20/15 to 12/8/15Or., Id., Ut., Mt.,Nv., Nd.. Wy.203328TF Crunchy Chinese Chicken Recovery 2ct Salad KitBulk KitAlbertsonsTF 313, 314, 315, 316, 317, 318, 320, 321, 322, 324, 32742511/20/15 to 12/8/15Or., Id., Ut., Mt.,Nv., Nd.. Wy.215305Sig Cafe Chicken Bacon Ranch Pasta 2Cnt Salad KitBulk KitSafewayTF 313, 317, 320, 324, 325, 326, 32829811/20/15 to 12/8/15Co., Wy., Sd., Ne.203119TF Apple Waldorf 2ct Salad KitBulk KitSafeway/ AlbertsonsTF 314, 317, 321, 324, 325, 326, 327, 32820811/20/15 to 12/8/15Co., Wy., Sd., Ne., Or.203136TF Crunchy Pea 2ct Salad KitBulk KitSafeway/ AlbertsonsTF 313, 314, 315, 316, 317, 318, 320, 321, 322, 324, 325, 326, 327, 32894411/20/15 to 12/8/15Wa.,Or.,Id.215350Celery Slcd 1/2" Diagonal 2/5# bagsFood Service BagSafewayTF 313, 314, 315, 316, 317, 319, 320, 321, 322, 323, 326, 327, 32823611/20/15 to 12/5/15Ca., Nv.270067TF Buffalo Chicken Burrito 1/11oz TrayTraySafewayTF 318, 319, 320, 321, 322, 323, 324, 325, 326, 327, 328243911/20/15 to 11/30/15Ca., Nv.279019Sig Cafe Thai Style W/Chicken Premade Salad 12oz TrayPremade SaladSafewayTF 318, 319, 320, 321, 322, 323, 324, 325, 326, 327, 3281872711/20/15 to 12/1/15Ca., Nv., Or.279028Sig Cafe Sriracha W/Chicken Premade Salad 8.75oz TrayPremade SaladSafewayTF 317, 318, 319, 321, 322, 323, 324, 325, 326, 327, 328772111/20/15 to 12/1/15Co., Wy., Sd., Ne.,Ca., Nv.203356TF Chinese Style Chicken Recovery 2Ct Salad KitBulk KitSafewayTF 313, 314, 315, 316, 317, 318, 319, 320, 321, 322, 323, 324, 325, 326, 327, 3282119

Wednesday, November 25, 2015

New #petfood #recall potential #salmonella contamination of Blue Buffalo Cub size wilderness wild chews

Blue Buffalo Voluntarily Recalls One Lot of Cub Size Wilderness Wild Chews Bones Due to Potential Salmonella Health Risk

Consumers: Bluebuffalo4260@stericycle.com or 888-641-9736

Product Distributed Since November 19 Through PetSmart Stores in 9 States; No Illnesses Reported

Blue Buffalo Company is voluntarily recalling one production lot of Cub Size Wilderness Wild Chews Bones. This is being done in an abundance of caution, as the product has the potential to be contaminated with Salmonella.

Salmonella can affect animals eating the product and there is risk to humans from handling contaminated pet products, especially if they have not thoroughly washed their hands after having contact with the products or any surfaces exposed to these products.

Healthy people infected with Salmonella should monitor themselves for some or all of the following symptoms: nausea, vomiting, diarrhea or bloody diarrhea, abdominal cramping and fever. Rarely, Salmonella can result in more serious ailments including arterial infections, endocarditis, arthritis, muscle pain, eye irritation and urinary tract symptoms. Consumers exhibiting these signs after having contact with this product should contact their healthcare provider.

Pets with Salmonella infections may have decreased appetite, fever and abdominal pain. Other clinical signs may include lethargy, diarrhea or bloody diarrhea, and vomiting. Infected but otherwise healthy pets can be carriers and infect other animals or humans. If your pet has consumed the recalled product and has these symptoms, please contact your veterinarian.

The product was distributed starting November 19, 2015 in PetSmart stores located in the following 9 states: California, Kansas, Michigan, Minnesota, Montana, Nevada, Oregon, Utah, and Washington. The recalled product comes individually shrink-wrapped in plastic with the UPC number 840243110087 printed on a sticker affixed to the product, and an expiration date of November 4, 2017, printed as “exp 110417” on the shrink-wrap. Consumers should look at the UPC Code and expiration date on the product package to determine if it is subject to the voluntary recall.

The voluntary recall is limited to the following product and production lot:

Product NameUPC CodeExpiration DateCub Size Wilderness Wild Chews Bone840243110087November 4, 2017

Routine testing at the manufacturing site revealed the presence of Salmonella in the product. No illnesses have been reported to date and no other Blue Buffalo products are affected.

Consumers who have purchased the product subject to this recall are urged to dispose of the product or return it to the place of purchase for full refund.

Consumers with questions may contact Blue Buffalo at: 888-641-9736 from 8 AM to 5 PM Eastern Time Monday through Friday and the weekend of November 28, 2015, or by email atBluebuffalo4260@stericycle.com for more information.

About Blue Buffalo

Blue Buffalo, based in Wilton, CT, is a pet products company that makes natural foods and treats for dogs and cats.

New #foodsafety #recall #undeclared #allergen of cashews & Almonds in Raley's Frozen Sweet Pumpkin Ravioli

Raley's Family of Fine Stores Issues Allergy Alert on Undeclared Cashew and Almond in Raley's Frozen Sweet Pumpkin Ravioli
Chelsea Minor, Director of Public Relations & Public Affairs 916-207-7060 :Raley's 1-800-925-9989 WEST SACRAMENTO, CA - Raley's Family of Fine Stores removed Raley's Frozen Sweet Pumpkin Ravioli 10 oz. from our Raley's, Bel Air and Nob Hill stores on November 17, 2015. According to the manufacturer, the product may contain an undeclared cashew and almond allergen. The UPC Code for the product is 046567021218 and the recall is for all lot numbers. There is no health risk associated with these products for individuals who are not allergic to cashews and/or almonds. Raley's is not aware of any injuries or illnesses reported to date associated with this product. Raley's cares about the health and safety of our customers. Customers who purchased the recalled product from our stores should return the product and Raley's will refund you for your purchase of this product in our stores. Additional information can also be found at our website www.raleys.comdisclaimer icon. Customers with questions or concerns may contact Raley's at 1-800-925-9989 FREE.

New #foodsafety #recall due to #misbranding and #undeclared #allergen of Boyle'S beef products

Boyle’S Famous Corned Beef Co. Recalls Beef Products Due to Misbranding and Undeclared Allergen

Class II Recall143-2015

Health Risk: Low
Nov 25, 2015

Congressional and Public Affairs
Katherine Scheidt
(202) 720-9113

WASHINGTON, Nov. 25, 2015 – Boyle’s Famous Corned Beef Co., a Kansas City, Mo. establishment, is recalling an undetermined amount of beef products due to misbranding and an undeclared allergen, the U.S. Department of Agriculture’s Food Safety and Inspection Service (FSIS) announced today. The product contains hydrolyzed wheat protein, a known allergen which is not declared on the product label.

The Beef Top Round was produced between Nov. 24, 2013 and Nov. 24, 2015. The following product is subject to recall: [View Label]

Approximately 20-lb. cases containing “Boyle’s FAMOUS USDA CHOICE SEASONED-COOKED BEEF TOP ROUND.”

The products subject to recall bear establishment number “EST. M-469” inside the USDA mark of inspection. The items were shipped to distributors in Iowa, Kansas and Missouri.

The problem was discovered by FSIS personnel while conducting allergen verification tasks. The inspector discovered that a seasoning pack containing hydrolyzed wheat protein was added into the product without listing wheat on the final product label.

There have been no confirmed reports of adverse reactions due to consumption of these products. Anyone concerned about an injury or illness should contact a healthcare provider.

Consumers who have purchased these products are urged not to consume them. These products should be thrown away or returned to the place of purchase.

FSIS routinely conducts recall effectiveness checks to verify recalling firms notify their customers of the recall and that steps are taken to make certain that the product is no longer available to consumers. When available, the retail distribution list(s) will be posted on the FSIS website at www.fsis.usda.gov/recalls.

Consumers and Media with questions about the recall can contact Gregg Ouverson, General Manager, at (816) 221-6284.

Consumers with food safety questions can "Ask Karen," the FSIS virtual representative available 24 hours a day at AskKaren.gov or via smartphone at m.askkaren.gov. The toll-free USDA Meat and Poultry Hotline 1-888-MPHotline (1-888-674-6854) is available in English and Spanish and can be reached from l0 a.m. to 4 p.m. (Eastern Time) Monday through Friday. Recorded food safety messages are available 24 hours a day. The online Electronic Consumer Complaint Monitoring System can be accessed 24 hours a day at:http://www.fsis.usda.gov/reportproblem.

USDA Recall ClassificationsClass IThis is a health hazard situation where there is a reasonable probability that the use of the product will cause serious, adverse health consequences or death.Class IIThis is a health hazard situation where there is a remote probability of adverse health consequences from the use of the product.Class IIIThis is a situation where the use of the product will not cause adverse health consequences.

Friday, November 20, 2015

New #foodsafety #recall #undeclared #peanut #allergen in Snickers 8x8 cake.

Casey's Bakery Inc. Issues Allergy Alert On Undeclared Peanuts in Snickers 8x8 Cake

FDA posts press releases and other notices of recalls and market withdrawals from the firms involved as a service to consumers, the media, and other interested parties. FDA does not endorse either the product or the company.

SHARETWEETMORE SHARING OPTIONSEMAIL

For Immediate Release

November 18, 2015

Contact

ConsumersKathy De Groot
 (301) 538-9682

Firm Press Release

View Product Photos

Casey's Bakery Inc. of Sioux Center, Iowa is voluntarily recalling all Snickers 8x8 cakes produced prior November 14, 2015, because the cakes contain undeclared peanuts. People who have an allergy or severe sensitivity to peanuts run the risk of serious or life-threatening allergic reaction if they consume these products.

Snickers 8x8 cake was distributed to stores in Orange City, Hartley and Hawarden by delivery to grocery stores. The cakes were also sold out of the Casey's Bakery retail store in Sioux Center. The cakes were only distributed within the state of Iowa.

All cakes with date codes prior to 696 or purchased before Nov. 14, 2015 are being recalled. The code may be found on the back of the product package. Cakes come in individual foil trays with clear plastic lids and are sold frozen. Net weight is 23 oz.

No Illnesses have been reported to date.

The recall was voluntarily initiated after a label inspection was performed and it was discovered the label did not properly claim peanuts in the toppings as an ingredient. The labeling has been updated and all current Snickers 8x8 cakes properly declare the peanuts in the toppings on the Ingredient List.

This recall does not apply to any other Casey's Bakery Products.

Consumers may return the product to Casey's Bakery Inc. for a full refund. For more information, contact Kathy De Groot at 712-722-2551 9 am to 5 pm CST Monday through Friday.

Thursday, November 19, 2015

New #foodsafety #recall #misbranding & #undeclared #allergen of soy in Mama Cozzi’s Pizza Kitchen Products

Nation Pizza Recalls Mama Cozzi’s Pizza Kitchen Products Due To Misbranding and Undeclared Allergens

Class II Recall142-2015

Health Risk: Low

Nov 19, 2015

Congressional and Public Affairs
Julie Schwartz
(202) 720-9113

WASHINGTON, Nov. 19, 2015 – Nation Pizza, a Schaumburg, Ill. establishment, is recalling approximately 59,028 pounds of frozen Mama Cozzi’s Pizza Kitchen products due to misbranding and undeclared allergens, the U.S. Department of Agriculture’s Food Safety and Inspection Service (FSIS) announced today. The products contain soy, a known allergen which is not declared on the product label.

The Mama Cozzi’s Pizza Kitchen Rising Crust Pepperoni Pizzas were produced between Aug. 25, 2015, and Nov. 9, 2015. The following products are subject to recall: [Labels(PDF Only)]      

27.5 ounce carton containing one “MAMA COZZI’S RISING CRUST PEPPERONI PIZZA.”

The products subject to recall bear establishment number “EST. 1682A” inside the USDA mark of inspection. These items were shipped exclusively to ALDI grocery stores in Indiana, Ohio, Pennsylvania, and Tennessee.                                

The problem was discovered during in-plant review activities.

There have been no confirmed reports of adverse reactions due to consumption of these products. Anyone concerned about an injury or illness should contact a healthcare provider.

Consumers who have purchased these products are urged not to consume them. These products should be thrown away or returned to the place of purchase.

FSIS routinely conducts recall effectiveness checks to verify recalling firms notify their customers of the recall and that steps are taken to make certain that the product is no longer available to consumers.

Consumers with questions about the recall can contact Teresa Martinez, Vice President of Quality Assurance, Research & Development, at (847) 348-5433. Media with questions about the recall can contact Richard Auskalnis, President, at (847) 348-5454.

New #dietary #supplement #recall due to #undeclared #sibutramine

Fit Firm and Fabulous Issues Voluntary Nationwide Recall of Ultimate Herbal Slimcaps Due to the Presence of Undeclared Sibutramine

Consumers: Mark Harris
Email - customerservice@fitfirmandfabulous.com
267-721-5585

Fit Firm and Fabulous is voluntarily recalling lots 05/02/2015 to 05/01/2017 of Ultimate Herbal Slimcap capsules, to the consumer level. FDA analysis has found the product to contain undeclared sibutramine. Sibutramine was a previously approved controlled substance that was removed from the U.S. market in October 2010 for safety reasons. This ingredient makes Ultimate Herbal Slimcap an unapproved drug for which safety and efficacy have not been established and, therefore, subject to recall.
Products containing sibutramine pose a threat to consumers because sibutramine is known to substantially increase blood pressure and/or pulse rate in some patients and may present a significant risk for patients with a history of coronary artery disease, congestive heart failure, arrhythmias or stroke. These products may also interact in life threatening ways with other medications a consumer may be taking. To date, Fit Firm and Fabulous has not received any reports of adverse events related to this recall.

The product is a dietary supplement marketed for weight loss and is packaged in 30-count bottles, labeled Part 1 of 3, UPC 5 42423 25422 1. The affected Ultimate Herbal Slimcap lots include the following lots 05/02/2015 to 05/01/2017. The product can be identified by. Ultimate Herbal Slimcaps was distributed Nationwide via the website.

Fit Firm and Fabulous has notified its distributors and customers by telephone and has arranged for return or destroy of all recalled products. Consumers/distributors/retailers that have product which is being recalled should stop using and discard.

Consumers with questions regarding this recall can contact Fit Firm and Fabulous by e-mail at customerservice@fitfirmandfabulous.com on Monday through Friday from 9 am EST and 5 pm EST Consumers should contact their physician or healthcare provider if they have experienced any problems that may be related to taking or using this drug product.

Adverse reactions or quality problems experienced with the use of this product may be reported to the FDA's MedWatch Adverse Event Reporting program either online, by regular mail or by fax.

Complete and submit the report Online: www.fda.gov/medwatch/report.htm
Regular Mail or Fax: Download form www.fda.gov/MedWatch/getforms.htm or call 1-800-332-1088 to request a reporting form, then complete and return to the address on the pre-addressed form, or submit by fax to 1-800-FDA-0178.
This recall is being conducted with the knowledge of the U.S. Food and Drug Administration.

Wednesday, November 18, 2015

New #foodsafety #recall due to #undeclared #allergen of #treenuts in Wegmans Italian Classics Butternut Squash Ravioli, 9 oz

Wegmans Food Markets Issues Allergy Alert on Undeclared Tree Nuts (Cashews and Almonds) in Wegmans Italian Classics Butternut Squash Ravioli, 9 oz.

Consumers: Wegmans Food Markets, Inc. 1-855-934-3663

Wegmans Food Markets, Inc. is recalling Wegmans Italian Classics Butternut Squash Ravioli, 9 oz. (UPC #77890 36434), because the product may contain undeclared cashews and almonds. People who have an allergy or severe sensitivity to cashews or almonds run the risk of serious or life-threatening allergic reaction if they consume this product.
Approximately 54,000 units of Wegmans Italian Classics Butternut Squash Ravioli, 9 oz. was sold in 88 Wegmans stores located in New York, New Jersey, Pennsylvania, Virginia, Maryland, and Massachusetts. This product, packaged in a plastic tray, is sold in a refrigerated case in the dairy department. All date codes sold since June 6, 2015 are included in the recall.

There have been no injuries or illnesses reported to date associated with this product. The recall was initiated because Wegmans was notified by the manufacturer that product testing showed the presence of almonds and cashews not declared on the label.

Wegmans will place automated phone calls to customers who purchased the product using their Shoppers Club card.

Customers who purchased the recalled product from Wegmans should return it to the service desk for a full refund. Consumers with questions may contact Wegmans consumer affairs department toll free at 1-855-934-3663 Monday through Friday, between 8:00 a.m. and 5:00 p.m. Eastern time.

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Wegmans Food Markets, Inc. is an 88-store supermarket chain with stores in New York, Pennsylvania, New Jersey, Virginia, Maryland, and Massachusetts. The family-owned company, founded in 1916, is recognized as an industry leader and innovator. Wegmans has been named one of the '100 Best Companies to Work For' by FORTUNE magazine for eighteen consecutive years. In 2015, Wegmans ranked #7 on the list. The company also ranked #1 for Corporate Reputation, among the 100 'most-visible companies' nationwide in the 2014 Harris Poll Reputation Quotient ® study.

New #foodsafety #recall due to #undeclared #allergen of #Milk in Honey Mustard Pretzel Mix and Honey Mustard Mix

Ashdon Farms Issues Allergy Alert on Honey Mustard Pretzel Mix and Honey Mustard Mix

Consumers: Ashdon Farms 800-274-3666

Ashdon Farms, Waukesha, WI 53188 is alerting consumers that Honey Mustard Pretzel Mix sold under the Girl Scouts of the USA brand and Honey Mustard Mix sold under the Ashdon Farms brand distributed to consumers on or before November 15, 2015 are being recalled because milk is not declared in the contains statement on the label. People with an allergy to milk should not consume these products. People who have an allergy or severe sensitivity to milk run the risk of serious or life threatening allergic reaction if they consume these products.
Girl Scouts of the USA branded product packaged in 7 oz bags (no UPC code) has been sold through Girl Scout Councils and online sales nationwide. Ashdon Farms branded product in 8 oz bags (UPC 79113-41184) has been sold through fund raising distributors nationwide. Ashdon Farms is currently correcting the label at the distribution level so that all product distributed to consumers on or after Nov 16, 2015 will correctly declare the milk allergen. ONLY PRODUCT DISTRIBUTED TO CONSUMERS ON OR BEFORE NOVEMBER 15, 2015 IS AFFECTED.

Due to correction at the distribution level the product cannot be identified based on code date. Affected packages can be identified by the contains statement found immediately below the ingredient listing. The contains statement on incorrect labels reads “Contains: Cashews, Almonds, Soy, Wheat.” Packages with the correct label read “Contains: Cashews, Almonds, Soy, Wheat, Milk.”

There have been no reports of illness or injury associated with this product.

Milk allergic consumers who have purchased the product may contact Ashdon Farms at 800-274-3666.

New #cattle #feed #recall of Kountry Buffet and Provider Pellet Products Due to Excessive Copper

CHS Inc. Issues Voluntary Recall of Certain Kountry Buffet and Provider Pellet Products Due to Excessive Copper

Consumers: CHS Inc. (800) 398-0327

CHS Inc. announced today it has implemented a voluntary recall of 50-pound packages of its Kountry Buffet 14% Text and Provider 15% Pellet, both for Mature Cattle, Horses, Goats & Sheep due to excessive levels of copper.
No illnesses or deaths have been reported to date. Consumption of the affected product may cause potential health risks, including death, in sheep. Symptoms of copper toxicity in sheep include lethargy, anemic appearance, excessive teeth grinding, extreme thirst, pale membranes (jaundice) and bloody urine.

The recalled products were manufactured in September 2015 and October 2015 at CHS Inc.'s Harrisburg, Ore., feed mill and distributed to 42 customers in Oregon and Washington. Kountry Buffet 14% Text features a salmon-colored label attached to a brown bag. Provider 15% Pellet features a yellow label attached to a brown bag. Affected Lot numbers for either product can be found at the bottom of the label and are as follows:

Kountry Buffet 14% Text Lot # Provider 15% Pellet Lot #
85092415-M702660 85101415-M732580
85100615-M720130 85101515-M734810
85101215-M728050
85101515-M734590
85102315-M748470
The potential presence of high copper levels was detected by routine sample tests of the product conducted by a third-party lab. After notifying the U.S. Food and Drug Administration in early November, the company began to proactively contact affected dealers and end consumers to inform each of the voluntary recall of all unconsumed product in the listed Lot numbers.
Consumers who purchased this product and have remaining quantities should immediately discontinue use and are urged to return them to the place of purchase for a full refund. Consumers with questions may contact the company at (800) 398-0327 between 8 a.m. and 5 p.m. CDT. Information also is available at http://www.paybacknutrition.com.

CHS Inc. (www.chsinc.com) is a leading global agribusiness owned by farmers, ranchers and cooperatives across the United States. Diversified in energy, grains and foods, CHS is committed to helping its customers, farmer-owners and other stakeholders grow their businesses through its domestic and global operations. CHS, a Fortune 100 company, supplies energy, crop nutrients, grain marketing services, animal feed, food and food ingredients, along with business solutions including insurance, financial and risk management services. The company operates petroleum refineries/pipelines and manufactures, markets and distributes Cenex® brand refined fuels, lubricants, propane and renewable energy products.

Tuesday, November 17, 2015

New #medical #device #recall of all Custom Ultrasonics Automated Endoscope Reprocessors from Healthcare facilities

FDA Orders Recall under Consent Decree for all Custom Ultrasonics Automated Endoscope Reprocessors

The U.S. Food and Drug Administration today ordered Custom Ultrasonics to recall all of its automated endoscope reprocessors (AERs) from health care facilities due to the firm's continued violations of federal law and a consent decree entered with the company in 2007. The identified violations could result in an increased risk of infection transmission. The FDA ordered this recall under the terms of the consent decree. The agency also issued a safety communication today recommending that health care facilities currently using Custom Ultrasonics AERs transition away from their use to alternative methods to reprocess flexible endoscopes as soon as possible.
These actions are part of the FDA's commitment to patient safety and ongoing efforts to minimize the risk of patient infections associated with reprocessed endoscopes, including duodenoscopes and scope accessories. The FDA has been working with federal partners, manufacturers and other stakeholders to better understand the critical factors contributing to bacterial infections associated with duodenoscopes and how to best mitigate them.

An estimated 2,800 AERs manufactured by Custom Ultrasonics are currently in hospitals and outpatient clinics throughout the United States. The FDA's recall order applies to all Custom Ultrasonics AERs, including the System 83 Plus, System 83 Plus 2 and System 83 Plus 9. Within seven business days after receiving the FDA's recall order, Custom Ultrasonics must provide a written recall proposal to the FDA.

"We are taking action because Custom Ultrasonics failed to meet its legal and regulatory obligations," said William Maisel, M.D., M.P.H., deputy director for science and chief scientist in the FDA's Center for Devices and Radiological Health. "The FDA's recall order stemmed from the company's continued violations of federal law and the consent decree and is necessary to protect the public health."

AERs are Class II medical devices that require 510(k) clearance and are used to wash and high-level disinfect endoscopes to decontaminate them between uses. AERs are designed to expose outside surfaces as well as interior channels of endoscopes to chemical solutions in order to kill microorganisms and prevent the spread of infection from these reusable medical devices. An endoscope must be thoroughly cleaned to remove any visible debris prior to placing it in an AER, which includes manually scrubbing the elevator mechanism and the recesses surrounding the elevator mechanism.

In 2012, under the terms of the consent decree, the FDA ordered Custom Ultrasonics to stop manufacturing and distributing all AER device models and components, and ordered their recall after the company failed to obtain FDA clearance following a significant change to the software operating system for one of its AERs. After Custom Ultrasonics obtained clearance for the significant change to the software operating system, the cleared devices were permitted to remain on the market. Since the 2012 order, the FDA has not authorized Custom Ultrasonics to resume manufacturing or distributing any AERs, though the company has continued to service them.

The FDA's most recent inspection of Custom Ultrasonics' facility in April 2015 documented continued violations. Violations include the inability to validate that the AERs can adequately wash and disinfect endoscopes to mitigate the risk of patient infection. In the months following the inspection, the FDA provided the company with an opportunity to correct inspection violations and requested additional validation data. Following a review of the company's submissions, the agency determined that Custom Ultrasonics has not adequately addressed its continued violations, which could result in an increased risk of infection transmission to patients.

Accordingly, under the terms of the consent decree, the agency today ordered Custom Ultrasonics to recall all of its AER devices.

The safety communication issued by the FDA today recommends that health care facilities currently using Custom Ultrasonics AERs transition away from their use to alternative methods to reprocess flexible endoscopes as soon as possible. The safety communication is based on both the recent violations of the law and consent decree and reports that endoscopes reprocessed by Custom Ultrasonics' AERs have been used in health care facilities that reported the transmission of serious bacterial infections. Specifically, the FDA advises health care facilities currently using a Custom Ultrasonics AER to take the following actions:

Identify and transition to alternate methods to reprocess flexible endoscopes, such as manual high-level disinfection, liquid chemical sterilization, alternative AERs or other cleaning and sterilization methods according to the endoscope manufacturer's reprocessing instructions.
Before transitioning to an alternative method, verify that the endoscopes used by the facility are compatible with the alternative method by referring to the endoscope manufacturer's reprocessing instructions.
Submit a report to Custom Ultrasonics and to the FDA via MedWatch if the health care facility suspects that a Custom Ultrasonics AER has caused or contributed to patient infection.
The FDA, an agency within the U.S. Department of Health and Human Services, protects the public health by assuring the safety, effectiveness, and security of human and veterinary drugs, vaccines and other biological products for human use, and medical devices. The agency also is responsible for the safety and security of our nation's food supply, cosmetics, dietary supplements, products that give off electronic radiation, and for regulating tobacco products.

New #foodsafety #recall possible #adulteration of Tyson chicken product.

Tyson Foods Inc. Recalls Chicken Product Due To Possible Adulteration

Class II Recall 141-2015
Health Risk: Low Nov 17, 2015
Congressional and Public Affairs
Gabrielle N. Johnston
(202) 720-9113

WASHINGTON, Nov. 17, 2015 – Tyson Foods Inc., a Pine Bluff, Ark. establishment, is recalling approximately 52,486 pounds of chicken wing product that may be adulterated because of having an “off odor” scent, the U.S. Department of Agriculture’s Food Safety and Inspection Service (FSIS) announced today.

The fully cooked buffalo style chicken wing section item was produced on October 24, 2015 and October 25, 2015. The following product is subject to recall: [Labels (PDF Only)]

28-oz. retail bags containing multiple pieces of “Tyson® Any’tizers® Fully Cooked Hot Wings® CHICKEN WING SECTIONS COATED WITH A FLAVORFUL HOT, TANGY SAUCE” with use by/sell by dates of October 24, 2016 and October 25, 2016, packaging dates 2975PBF0508-23/2985PBF0500-01 and case codes 2975PBF0508-23/2985PBF0500-01.
The product subject to recall bear establishment number “P-13456” inside the USDA mark of inspection as well as on the back of the bag above the heating instructions. These items were shipped to retail locations nationwide.

The problem was discovered when Tyson Foods Inc. received consumer complaints about the product being “off-odor” as well mild illness associated with consumption. After these consumer complaints, Tysons Food Inc. brought this to the attention of FSIS.

There have been no confirmed reports of adverse reactions due to consumption of these products by FSIS. Anyone concerned about an injury or illness should contact a healthcare provider.

Consumers who have purchased these products are urged not to consume them. These products should be thrown away or returned to the place of purchase.

FSIS routinely conducts recall effectiveness checks to verify recalling firms notify their customers of the recall and that steps are taken to make certain that the product is no longer available to consumers.

Media with questions about the recall can contact Derek Burleson, Public Relations Manager, (479) 290-6466. Consumers with questions about the recall can contact Tyson Foods’ Consumer Relations, (toll free) 866-328-3156.

Sunday, November 15, 2015

Beware fake news reports about recalled food products.

There is a fake news site stating that the Patti Labelle Sweet Potatoe Pie has killed numerous people. This news account is from a fake website. No such recall is currently listed, and the deaths have not happened.

http://www.hoax-slayer.net/fake-news-report-claims-hundreds-dead-after-eating-patti-labelle-pie/

Friday, November 13, 2015

New #foodsafety #recall undeclared #allergen of #peanuts in Pecan turtedoves Chocolate caramel pecan clusters

Virginia Diner, Inc. Issues Allergy Alert on Undeclared Peanut Allergen in Pecan Turtledoves Chocolate Caramel Pecan Clusters (Candy)

Consumers: Virginia Diner 800-935-4004

Wakefield, VA - Virginia Diner, Inc. is voluntarily recalling, as a precaution, 10 oz. cans of Happy Holidays Pecan Turtledoves Chocolate Caramel Pecan Clusters (Candy) at the company's Wakefield, VA location because they may contain peanuts and peanut allergens. People who have an allergy or severe sensitivity to peanuts run the risk of serious or life-threatening allergic reaction if they consume these products. This problem was discovered by a consumer who received and opened a Pecan Turtledove can and found Peanut Turtledoves within.
The Virginia Diner, Inc. is working with the U.S. Food and Drug Administration in administering this voluntary recall. The Virginia Diner has not received any reports of illness or injury to date regarding this product.

Only the following PRODUCT and LOT CODE is affected, found on the bottom of each can:

UPC Code: 0 85582 01155 2
Weight: 10 oz
Package Type: Can
Label: Happy Holidays Pecan Turtledoves Chocolate Caramel Pecan Clusters
Lot Code: 092915 PNT
BEST BY: 09 23 16

The recall does not apply to any other Virginia Diner branded products.

These Pecan Turtledoves were sold and distributed via fundraising organizations between September 30, 2015 and November 5, 2015. Participants accepted pre-orders on order forms, turned the completed forms in to the organization, which then turned the complete groups order in to the Virginia Diner for fulfillment. Orders were packed and shipped back to the organization for distribution within this 9/30/15-11/05/15 time frame. Each participant delivered the products to the end buyer. The Virginia Diner, Inc. is contacting affected groups and customers who may have received this mislabeled product, and are providing a list of participants of each group to be contacted. Consumers should return the product to the organization from which it was purchased for a replacement.

Additionally, orders were entered by the end consumer on the www.virginiadiner.comdisclaimer icon website. The web orders were shipped directly to the consumer. Each buyer has been contacted via phone and/or email.

Consumers who may have questions or concerns should contact the Virginia Diner at 800-935-4004, Monday through Friday, 9am to 5pm EDT

New #foodsafety #recall undeclared milk #allergen in Giant Eagle Apricot Logs and Poppyseed Logs

Giant Eagle Voluntarily Recalls Apricot Logs and Poppyseed Logs Due to an Undeclared Milk Allergen

FDA posts press releases and other notices of recalls and market withdrawals from the firms involved as a service to consumers, the media, and other interested parties. FDA does not endorse either the product or the company.

SHARETWEETMORE SHARING OPTIONSEMAIL

For Immediate Release

November 12, 2015

Contact

Consumers

800-553-2324

Media

Dan Donovan (412) 967-4551

Email: media.relations@gianteagle.com

Firm Press Release

View Product Photos

All lots of Market District brand Apricot Logs and Poppyseed Logs prepared and sold individually from the Bakery department inside Giant Eagle and Market District supermarkets with sell by dates from November 7, 2015 through November 17, 2015 have been voluntarily recalled by Giant Eagle due to an undeclared milk allergen.  People who have an allergy or severe sensitivity to milk run the risk of a serious or life-threatening allergic reaction if they consume these products. The product is safe for consumption by those who do not have milk allergies.

Approximately 460 potentially affected Apricot Logs and Poppyseed Logs were purchased in various transactions in Giant Eagle and Market District supermarkets in Pennsylvania, Ohio, West Virginia and Maryland. There are no reported illnesses to date associated with this recall.

The logs were sold individually from the Bakery department with UPCs of:

219772 509998                   Market District Apricot Log219773 509997                   Market District Poppyseed Log

Giant Eagle became aware of the issue after a quality assurance review of the ingredient declaration. The product label for the bakery logs, which contain milk, omitted milk as an allergen.

Customers with a milk allergy who have purchased the affected product should dispose of it or return it to their local Giant Eagle or Market District store for a refund.  Customers with questions may call Giant Eagle Customer Care at 1-800-553-2324 Monday through Friday 9 a.m. to 9 p.m. EST.

In addition to this public communication regarding this recall, Giant Eagle initiated its consumer recall telephone notification process. The consumer recall process uses purchase data and consumer telephone numbers housed in the Giant Eagle Advantage Card® database to alert those households that purchased the affected product and have updated telephone contact information in the database.

Thursday, November 12, 2015

New #foodsafety #recall possible #choking #hazard in SpaghettiOs Original 14.2 oz cans.

SpaghettiOs Original 14.2oz Cans Recalled Due to Potential Choking Hazard

Consumers:  1-866-535-3774

Campbell Soup Company (NYSE:CPB) is voluntarily recalling 14.2 ounce cans of SpaghettiOs Original due to a potential choking hazard posed by pieces of red plastic found in a small number of cans. This plastic material is from parts of the can lining which may peel off.
The affected 14.2 ounce SpaghettiOs Original product has a date of February 22, 2017 which is stamped on the base of the can, and a UPC code of 51000 22432 printed under the bar code.

The issue was identified after the company received consumer complaints.

This recall affects 355,000 cans and is limited to the United States.

This product should not be eaten. People who have bought the affected product should return it to the store where it was purchased for an exchange or full refund. For more information call 1-866-535-3774 between 9 a.m. to 7 p.m. EST, Monday to Friday or visit Facebook/SpaghettiOs. Campbell Soup Company apologizes for the inconvenience.

About Campbell Soup Company

Campbell (NYSE:CPB) is driven and inspired by our Purpose, “Real food that matters for life’s moments.” The company makes a range of high-quality soups and simple meals, beverages, snacks and packaged fresh foods. For generations, people have trusted Campbell to provide authentic, flavorful and readily available foods and beverages that connect them to each other, to warm memories, and to what’s important today. Led by its iconic Campbell’s brand, the company’s portfolio includes Pepperidge Farm, Bolthouse Farms, Arnott’s, V8, Swanson, Pace, Prego, Plum, Royal Dansk, Kjeldsens and Garden Fresh Gourmet. Founded in 1869, Campbell has a heritage of giving back and acting as a good steward of the planet’s natural resources. The company is a member of the Standard & Poor’s 500 and the Dow Jones Sustainability Indexes. For more information, visit www.campbellsoupcompany.com or follow company news on Twitter via @CampbellSoupCo.

New #foodsafety #recall possible #salmonella contamination of Homestat Farm: Organic Steel Cut Oats & Chia With Flax And Rye Flakes

Homestat Farm Recalls Organic Steel Cut Oats & Chia With Flax And Rye Flakes Because Of Possible Health Risk

Consumers: Homestat Farm  1-800-819-3918

Homestat Farm of Dublin, OH is recalling some of its 42-ounce packages only of "Organic Steel Cut Oats & Chia with Flax And Rye Flakes" because the flax seed ingredient has the potential to be contaminated with Salmonella, an organism which can cause serious and sometimes fatal infections in young children, frail or elderly people, and others with weakened immune systems. Healthy persons infected with Salmonella often experience fever, diarrhea (which may be bloody), nausea, vomiting and abdominal pain. In rare circumstances, infection with Salmonella can result in the organism getting into the bloodstream and producing more severe illnesses such as arterial infections (i.e., infected aneurysms), endocarditis and arthritis.
The recalled "Organic Steel Cut Oats & Chia with Flax And Rye Flakes" was distributed on a limited basis in Sams Club retail stores located in AK, CA, FL, GA, IL, IN, KS, MD, MI, MN, MS, NC, NH, OH, PA & TX.

The product comes in a 42 ounce carton UPC 8 35882 00620 4 marked with Best Buy: 03/16/17-1, 03/16/18-1, 03/19/17-1, 03/19/17-2, 03/23/17-1, 03/23/17-2, 03/24/17-1, 03/26/17-1, 03/26/17-2, 04/08/17-2. The best buy date can be found embossed on the bottom flap of box next to the bar code.

No illnesses have been reported to date in connection with this issue.

A supplier informed Homestat Farm of this after a contamination was found in flax seed provided to another customer.

Consumers who have purchased these 42-ounce packages of "Organic Steel Cut Oats & Chia with Flax And Rye Flakes" should return them to the place of purchase for a full refund. Consumers with questions may contact the company at 1-800-819-3918 M-F 10AM-4PM.

Looks like a new #foodsafety #recall will be coming soon involving a choking hazard in cans of #Spaghettios.

Looks like a new #foodsafety #recall will be coming soon involving a choking hazard in cans of #Spaghettios.

http://www.nbcnews.com/business/consumer/uh-oh-recall-after-choking-hazard-found-spaghettios-cans-n462521?cid=sm_tw&hootPostID=3c1ddc60052b09636b048d52a8ab1eec&cid=sm_fb

New #foodsafety #recall undeclared tree nut #allergen in Trader Joe's Trader Giotto's Butternut Squash Triangoli

Trader Joe’s Issues Voluntary Allergy Alert on Tree Nuts In Trader Giotto’s Butternut Squash Triangoli

Consumers: Alison Mochizuki
  amochizuki@traderjoes.com
 (626) 599-3779

Trader Joe’s of Monrovia, California is voluntarily recalling Trader Giotto’s Butternut Squash Triangoli (UPC 00943482/SKU 94348) sold in the refrigerated deli section with “Use or Freeze by” codes 04 16 15 through 01 15 16, because it may contain undeclared tree nuts. All affected product has been removed from store shelves. People who have an allergy or severe sensitivity to tree nuts run the risk of serious or life-threatening allergic reaction if they consume these products.

The Trader Giotto’s Butternut Squash Triangoli is packaged in an 8.8 oz. package, with code information printed on the upper-right corner of the front of the package. The product was distributed to Trader Joe’s stores nationwide. Trader Joe’s initiated the voluntary removal of this product after customers reported having an allergic reaction after consuming the product. The customers are allergic to tree nuts, which are not an intended ingredient in this product.

Customers who have purchased the Trader Giotto’s Butternut Squash Triangoli may return it to Trader Joe’s for a full refund. Customers with questions may contact Trader Joe’s customer relations at (626) 599- 3817, 6AM-6PM PST, Monday-Friday.

New #petfood #recall due to mold in Halo, Purely for Pets® Sensitive Cat Turkey Dry Food

Halo, Purely for Pets® Issues Voluntary Recall of Sensitive Cat Turkey Dry Food Due to Mold

Contact: Consumers 800-426-4256
Email: customers@halopets.com

Halo, Purely for Pets has initiated a limited, voluntary recall of its Spot’s Stew Sensitive Cat Turkey kibble with a Best By date of 09/04/2016 due to reports of mold. No other Halo products are affected.

Consumers who have Spot’s Stew Sensitive Cat Turkey stamped “Best By 09/04/2016” should discontinue feeding, and return the remaining portion to any Halo retailer for a full refund or replacement.

While some pets can ingest mold without incident, others may experience digestive issues. Consumers should consult their veterinarian if their cat experiences digestive issues.
Halo is also instructing its retailers to remove Sensitive Cat Turkey products stamped “Best By 09/04/2016” from their shelves.

The affected product is:

Product name:

Spot’s Stew Wholesome Turkey Recipe Sensitive Formula for Cats

UPC Codes:

745158350231 and 745158340232

Sizes:

6 lb. and 3 lb. bags

Best by Date:

09/04/2016


For more information, contact Halo Customer Care at 800-426-4256 Monday-Friday 8:00 a.m. – 5:00 p.m. EST, or emailcustomers@halopets.com or visitwww.halopets.com.

ABOUT HALO, PURELY FOR PETS®

For over 25 years, Halo, Purely for Pets® has created holistic pet products of uncompromising quality. Halo believes nutrition is the single most important factor in the quality of a pet’s life. When you choose Halo, we feed it forward, donating over 1.5 million meals to shelter pets annually, in partnership with Freekibble.com. Ellen DeGeneres – a long time Halo customer – became part-owner in 2008. In 2010, Halo donated 1 million meals to shelter pets for the U.S. Postal Service Adopt a Shelter Pet Stamp Program. Halo now sponsors the acclaimed PBS series “Shelter Me,” the Olate Dog Rescue Tour 2014-2015, LoveAnimals.org, and many more animal rescue efforts. Halo’s natural dog food, natural cat food, treats, supplements and grooming products are available at Petco, Sprouts, PetSmart Canada, and other fine pet specialty and natural food stores. Learn more at www.halopets.com.