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Safety Reports: Recall

Updated:

Real Time Reports

Gilead Sciences, Inc. issued a voluntary recall of one lot of Veklury® (remdesivir) for Injection to the consumer level. The product was distributed nationwide in the United States, beginning 16 July 2024

Risk Statement: The administration of an injectable product that contains glass particles may result in… See more

#recall #drugs #unitedstates

Bionpharma Inc. is voluntarily recalling (1) a single batch of Atovaquone Oral Suspension at the consumer level. The product was found to be contaminated with Cohnella bacteria. The affected batch of product was manufactured at CoreRx, Inc. and shipped nationwide to customers between December 21, 2023, and… See more

#drugs #recall #unitedstates

Dynarex Corporation is recalling Dynacare Baby Powder because it has the potential to be contaminated with asbestos. The product was sent to distributors on or after March 11, 2024, by direct delivery in the following states: AL, AR, CO, IL, KY, NC, NJ, PA, TN, FL, WA,… See more

#recall #cosmetics #unitedstates

The U.S. Consumer Product Safety Commission and Bestway (Hong Kong) International Ltd. have announced the recall of approximately 866,000 AirJet and HydroJet Spa Pumps because the product can overheat causing the plastic housing to ignite, posing a fire hazard. The recalled spa pumps were sold together with… See more

#recall #unitedstates

Breas Medical initiated a U.S. nationwide correction of 8,186 Vivo 45 LS ventilator devices. Internal testing of the ventilator identified the potential for short term elevated levels of formaldehyde exposure to users under specific conditions.

Short term formaldehyde emissions may lead to adverse pulmonary or neurological effects… See more

#recall #medicaldevices #unitedstates

312   Comments Comment
B. Braun Medical Inc. (B. Braun), is voluntarily recalling two (2) lots of 0.9% Sodium Chloride for Injection USP 1000 mL in E3 containers. The voluntary recall has been initiated due to the potential for particulate matter and fluid leakage of the respective containers. The product was… See more

#drugs #recall #unitedstates

312   Comments Comment
Baxter International Inc. is voluntarily recalling one lot of Heparin Sodium in 0.9% Sodium Chloride Injection to the consumer level due to the potential for elevated endotoxin levels based on issues related to the bacterial endotoxin test specific to lot number. This issue affects one lot of… See more

#recall #drugs #unitedstates

312   Comments Comment
Abbott has initiated a voluntary medical device correction for a small number of FreeStyle Libre® 3 sensors due to sensors may provide incorrect high glucose readings. The product was distributed in the United States during the first half of May 2024.

The FreeStyle Libre 3 system includes… See more

#recall #medicaldevices #unitedstates

312   Comments Comment
Aurobindo Pharma USA, Inc., on behalf of AuroHealth, is voluntarily recalling one lot of Healthy Living Migraine Relief, Acetaminophen, Aspirin & Caffeine tablets to the consumer level due to the product missing the manufacturer label. The product was distributed through Amazon to be known within the US… See more

#drugs #recall #unitedstates

312   Comments Comment
Main Products, Inc. is voluntarily recalling all lots of "Umary Acido Hialuronico, Suplemento Alimenticio to the consumer level. FDA laboratory analysis confirmed that UMARY has been found to be tainted with the drug ingredients, diclofenac and omeprazole. Products containing diclofenac and omeprazole cannot be marketed as dietary… See more

#dietarysupplements #recall #unitedstates

312   Comments Comment