Zingerman’s Creamery Issues Allergy Alert on Undeclared Egg in Paw Paw and Harvest Pumpkin Gelato

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Zingerman’s Creamery of Ann Arbor, MI is recalling 173 pints of Paw Paw Gelato, 50 quarts of Paw Paw Gelato, 58 pints of Harvest Pumpkin Gelato, 10 quarts of Harvest Pumpkin Gelato that are currently out in commerce because it may contain undeclared Egg allergen. People who have an allergy or severe

Source: FDA Food Safety Recalls RSS Feed

Mylan Institutional LLC, a Viatris Company, Issues a Voluntary Recall of One Lot of Octreotide Acetate Injection, 500 mcg/mL, Due to Glass Particulates in a Syringe

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Mylan Institutional LLC, a Viatris company, is voluntarily recalling lot AJ21002, exp 3/2024, of Octreotide Acetate Injection, 500 mcg/mL, packaged in a carton of ten 1mL syringes. This lot is being recalled at the user (hospital/pharmacy) level due to a product complaint of the presence of glass pa

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

Clorox® Recalls Pine-Sol® Scented Multi-Surface Cleaners, CloroxPro® Pine-Sol® All Purpose Cleaners, and Clorox® Professional™ Pine-Sol® Lemon Fresh Cleaners Due to Risk of Exposure to Bacteria

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The recalled products may contain bacteria, including Pseudomonas aeruginosa, an environmental organism found widely in soil and water. People with weakened immune systems or external medical devices who are exposed to Pseudomonas aeruginosa face a risk of serious infection that may require medical treatment. The bacteria can enter the body if inhaled, through the eyes, or through a break in the skin. People with healthy immune systems are usually not affected by the bacteria. 

Source: Recall List

Whele LLC Announces National Voluntary Recall of Mighty Bliss Electric Heating Pad Due to Product Safety Concerns

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Boston, MA, October 18, 2022 / PRNewswire / – Whele LLC, of Boston, MA, is voluntarily recalling its Mighty Bliss Electric Heating Pad, due to product safety concerns. Use of this product may lead to burns, mild shocks, or rashes/irritation

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

Aurobindo Pharma USA, Inc. Initiates Voluntary Nationwide Recall of Two (2) Lots of Quinapril and Hydrochlorothiazide Tablets USP 20mg/12.5mg, Due to the Detection of N-Nitroso Quinapril Impurity

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East Windsor, New Jersey, Aurobindo Pharma USA, Inc. has initiated a voluntary recall of two (2) lots (refer table below) of Quinapril and Hydrochlorothiazide Tablets USP 20mg / 12.5mg, to the consumer level from the US market due to presence of Nitrosamine Drug Substance Related Impurity (NDSRI), N

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

Sotto I Trulli, Inc. DBA Bombolo Biscotti Issues Allergy Alert on Undeclared Walnut in Product

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Sotto i Trulli INC/DBA Bombolo Biscotti, is recalling its Assorted Italian Cookies, because it contains Italian Wedding Cookies with undeclared walnut ingredient. People who have an allergy or severe sensitivity to walnut allergen, run the risk of serious or life-threatening allergic reaction if the

Source: FDA Food Safety Recalls RSS Feed

Seed Ranch Flavor Co Issues Allergy Alert on Undeclared Soy in “Umami Everyday Sauce” and “Everything But The Sushi & Dumplings” Sauce

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Seed Ranch Flavor Co. of Boulder, CO, is voluntarily recalling its 5 fl ounce bottles of "Umami Everyday Sauce" and “Everything But The Sushi & Dumplings” sauce because they contain undeclared soy. People who have allergies to soy run the risk of serious or life-threatening allergic reaction if they

Source: FDA Food Safety Recalls RSS Feed

Baxter Issues Urgent Medical Device Correction Regarding Potential Radio Frequency Interference With Other Devices Near Beds Installed With WatchCare System

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Baxter International Inc. announced today it has issued an Urgent Medical Device Correction for the WatchCare Incontinence Management System due to potential for radio frequency (RF) interference with other medical devices. The WatchCare system is designed to discreetly alert the caregiver of an inc

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

Juvo Plus Recalls Children’s Butterfly Net Sets and Army Action Figure Playsets Due to Violations of Federal Phthalates and Lead Content Bans (Recall Alert)

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Components of the recalled butterfly net sets and the action figure playsets contain levels of certain phthalates and lead that exceed the federal phthalate and lead content standards. Phthalates and lead are toxic if ingested by young children and can cause adverse health issues.

Source: Recall List

AQUALUNG Recalls Buoyancy Compensator Devices Due to Injury and Drowning Hazards

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The dump valve knob can get stuck when the recalled BCD is inflated, opening the dump valve which stops the BCD from fully inflating. This can result in a loss of buoyancy control and poses injury (decompression sickness) and drowning hazards.

Source: Recall List