Entries by Heather Davis

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

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...

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

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 ri...

Source: Recall List

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

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 Nitros...

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

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

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...

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

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 desi...

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)

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 ca...

Source: Recall List