Meijer Recalls Select Mixed Nuts due to Undeclared Brazil Nuts in Product

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Meijer is initiating a voluntary recall of 13,284 packages of mixed nuts due to the potential risk of an undeclared tree-nut allergen (Brazil nuts) sold at all Meijer stores, and is being issued to its customers in cooperation with the U.S. Food & Drug Administration.

Source: Food and Drugs Administration--Recalls/Safety Alerts

BD Provides Update on Feb. 4, 2020 Voluntary Recall of the BD Alaris™ System PC Units and Modules

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BD (Becton, Dickinson and Company) (NYSE: BDX), a leading global medical technology company, today provided an update on a previously announced voluntary recall of the BD Alaris™ System regarding software for the PC Unit and certain modules. BD has notified customers affected by this recall, and the

Source: Food and Drugs Administration--Recalls/Safety Alerts

Dole Fresh Vegetables, Inc. Announces Voluntary Limited Recall of H-E-B-branded Tuscan Herb Salad Kit Due to Undeclared Allergens

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This recall is due to possible undeclared allergens (peanut, wheat, soy and tree nuts) in H-E-B-branded Tuscan Herb Salad Kit, which was manufactured by Dole for H-E-B. The incorrect masterpack (kit with dressing and other toppings) was unintentionally used during the production of the salad.

Source: FDA Food Safety Recalls RSS Feed

Stonewall Kitchen Voluntarily Recalls a Limited Amount of Mislabeled Ghost Pepper Salsa which contains Ghost Pepper Queso

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Stonewall Kitchen of York, Maine is voluntarily recalling 4,812 jars of its Ghost Pepper Queso with an Enjoy By date of 23MAY2021, as a small number of those were mislabeled as Ghost Pepper Salsa. Ghost Pepper Queso includes two allergens, milk and soy, that are not included in Ghost Pepper Salsa, a

Source: FDA Food Safety Recalls RSS Feed

Hikma Pharmaceuticals USA Inc. Extends Voluntary Nationwide Recall of Ketorolac Tromethamine Injection, USP 30mg/mL, 1mL Fill/2mL Vials Due to the Potential Presence of Small Particulates

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Hikma Pharmaceuticals PLC (Hikma, Group), today announces that its subsidiary Hikma Pharmaceuticals USA Inc. (formerly known as West-Ward Pharmaceuticals Corp.; “Hikma”) is voluntarily extending its previously-announced recall of certain lots (listed below) of Ketorolac Tromethamine Injection USP 30

Source: Food and Drugs Administration--Recalls/Safety Alerts

Vita Food Products Issues Voluntary Recall of Mislabeled Vita Wild Herring Wine Sauce Containing Undeclared Milk

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Vita Food Products, Inc. of Chicago, Illinois is notifying the public that it is recalling up to 8,376 individual plastic jars of 32 ounce Vita Wild Herring in Wine Sauce that are potentially mislabeled because they may contain sour cream and, therefore, may contain undeclared milk.

Source: FDA Food Safety Recalls RSS Feed

Allergy Alert Issued for Undeclared Milk in Green Chile Chicken Tamales Sold at Whole Foods Market Stores in Multiple States

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Whole Foods Market is voluntarily recalling select Green Chile Chicken Tamales from stores across 24 states because they contain undeclared milk. 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.

Source: Food and Drugs Administration--Recalls/Safety Alerts

New Capstone, Inc. Issues Allergy Alert on Restructure Vanilla Protein Powder Due to Undeclared Milk

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New Capstone, Inc. of Mooresville, NC is recalling their 22oz ReStructure Vanilla Protein Powder pouches, Lot 19211 Exp. 06/21 and their 27 gram individual serving pouch, Lot 19211 Exp. 06/21, because they may contain undeclared milk.

Source: FDA Food Safety Recalls RSS Feed

Purina Animal Nutrition Voluntarily Recalling Select Lot Codes of Purina®Rabbit Feed, Purina® Turkey Feed, Country Acres® Rabbit Feed and DuMOR® Chick Starter/Grower Feed

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Purina Animal Nutrition is initiating a voluntary recall of multiple lots of Purina® Rabbit Feed, Purina® Turkey Feed, Country Acres® Rabbit Feed and DuMOR® Chick Starter/Grower Feed due to elevated calcium levels in the product.

Source: Food and Drugs Administration--Recalls/Safety Alerts

American Health Packaging Issues Voluntary Nationwide Recall of Ranitidine Tablets, USP 150 mg, 100 Count Unit Dose Blisters Due to the Detection of N-nitrosodimethylamine (NDMA) Impurity

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American Health Packaging has voluntarily recalled eleven (11) lots of Ranitidine Tablets, USP 150 mg, 100 count Unit Dose Blisters to the consumer level due to the potential N-Nitrosodimethylamine (NDMA) amounts above levels established by the FDA.

Source: Food and Drugs Administration--Recalls/Safety Alerts