Bazzini LLC Voluntarily Recalls Trader Joe’s Dark Chocolate Almond Butter Cup 2-Pak

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Bazzini LLC, Allentown, PA is, out of an abundance, voluntarily recalling three lot codes (SELL BY date codes of APR 05 2022, APR 06 2022, and APR 07 2022) of 1.4 ounce Trader Joe's Dark Chocolate Almond Butter Cups because it may contain peanut protein.

Source: FDA Food Safety Recalls RSS Feed

Bea Lydecker’s Naturals, Inc. Issues Allergy Alert on Undeclared Soy Lecithin in Living Free Dietary Supplement

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Bea Lydecker’s Naturals, Inc. of Oregon City, Oregon is recalling six Living Free brand dietary supplement products because labels declare lecithin but do not declare soy lecithin. People who have an allergy or severe sensitivity to soy should not consume these products.

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

Prairie Wolf Spirits, Inc. Issues Voluntary Nationwide Recall of Prairie Wolf Distillery Hand Sanitizer Packed in 16.9 Oz. and 20 Oz Bottles Because They Resemble Drink Containers

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Oklahoma City, Oklahoma, Prairie Wolf Spirits, Inc. is voluntarily recalling all lots of Prairie Wolf Distillery hand sanitizer packaged in 16.9 fluid ounce and 20 fluid ounce containers that resemble water bottles to the consumer level. The recall does not affect any other hand sanitizer product

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

Cuisine Solutions Issues Voluntary Recall of Flavored Plant-Based Bites

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Cuisine Solutions, Sterling, VA is initiating a voluntary recall of its JUST Egg flavored plant-based “bites” products due to undeclared allergens. A limited number of 2-pouch retail packages may contain an incorrect sealed pouch containing whole-egg and milk products. The interior plastic pouches

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

Sanit Technologies Adds Label Clarification to Existing Voluntary Hand Sanitizer Recall

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Sanit Technologies LLC d/b/a Durisan, is providing an additional 5 label illustrations and product sizes for customers that might not have been able to clearly identify containers of Non-Alcohol Hand Sanitizer products that were added to the voluntary recall initiated on March 24, 2021, and expanded

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

Smiths Medical Issues Worldwide Notification Regarding the Recall of Jelco® Hypodermic Needle-Pro® Fixed Needle Insulin Syringe With Skewed Graduation Markings

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Smiths Medical has become aware of specific models and lots of Jelco® Hypodermic Needle-Pro® Fixed Needle Insulin Syringes that may exhibit skewed odd number line graduation markings on their syringe barrels. Markings skewed approximately 20 degrees upward have been identified.

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

Designed By Nature Voluntarily Recalls Goat’s Milk, Cow’s Milk and Base Milk Formulas Due to Possible Health Risk

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DESIGNED BY NATURE of California is recalling our Goat’s Milk Powder, Cow’s Milk Powder and Base Milk Powder formulas with an expiration date between May 01, 2021 thru June 11, 2022. We intend to change our labeling to make it clear that these products are not intended to be used as infant formula

Source: FDA Food Safety Recalls RSS Feed

Philips Issues a Recall Notification* to Mitigate Potential Health Risks Related to the Sound Abatement Foam Component in Certain Sleep and Respiratory Care Devices

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Following the company update on April 26, 2021, Royal Philips(NYSE: PHG; AEX: PHIA) today provides an update on the recall notification* for specific Philips Bi-Level Positive Airway Pressure (Bi-Level PAP), Continuous Positive Airway Pressure (CPAP), and mechanical ventilator devices to address ide

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

Freshpet Voluntarily Recalls One Lot of Freshpet® Select Small Dog Bite Size Beef & Egg Recipe Dog Food Due to Potential Salmonella Contamination

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Freshpet Inc. is announcing a voluntary recall of a single lot of Freshpet® Select Small Dog Bite Size Beef & Egg Recipe Dog Food (1 LB bags), with Sell by Date 10/30/2021, due to potential contamination with Salmonella. Our Freshpet Team had designated this single lot for destruction, but it was in

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

Viona Pharmaceuticals Inc., Issues Voluntary Nationwide Recall of Metformin HCl Extended-Release Tablets, USP 750 mg, Due to the Detection of N-Nitrosodimethylamine (NDMA) Impurity

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Viona Pharmaceuticals Inc., is voluntarily recalling 2 (two) lots of Metformin Hydrochloride Extended-Release Tablets, USP 750 mg to the retail level.

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