Biocon Prazosin Hydrochloride 2 mg Capsules Recalled for Nitrosamine Impurity (58,896 bottles, 2026)
cGMP deviation: detection of Nitrosamine Drug Substance-Related Impurities, N-nitroso-prazosin impurity C (NNP) above acceptable limits.
2,756 recalls tagged with “immediate action”.
cGMP deviation: detection of Nitrosamine Drug Substance-Related Impurities, N-nitroso-prazosin impurity C (NNP) above acceptable limits.
Zarlengo Italian Ice recalls 173 one-gallon gelato buckets sold in Illinois, Indiana and Texas. Soy lecithin appears in ingredients but is not listed in the contains statement. Consumers should not consume this product and should seek refund or replacement.


Soy Lecithin listed in ingredients statement, but Soy is not mentioned in the contains statement.


CCCEI Brand power strips are recalled after a potential fire risk due to missing overcurrent protection. The recall covers 6ft, 10ft, and 15ft models sold by Middle Way Electronics. Consumers should stop using the product and request a full refund.

FUNTOK 24V 2-Seater Ride-On Trucks recalled by Shenzhen Luobe Trading Co. for fire and burn hazards. The recall covers model DLS-K03 sold in red, black, white and pink. The company urges consumers to stop using the product and contact for a full refund.

This recall involves MPINOI-branded adult portable bed rails. The white metal bed rails measure about 15 inches wide by 26 inches tall and have an extendable handle with gray padding and a black storage mesh pocket. "MPINOI" is printed on the mesh pocket.

Nexgrill recalls more than 10.2 million metal wire bristle grill brushes sold at Home Depot. Bristles can detach and stick to food or grills. Consumers should stop using recalled brushes and contact Nexgrill for a full refund issued as a gift card.



Lack of Assurance of Sterility
May be temperature abused, which may result in growth of Clostridium botulinum
Lack of Assurance of Sterility; blue Break-Off-Part could detach from the administration port
Lack of Assurance of Sterility; blue Break-Off-Part could detach from the administration port
Teva-affiliated Clonidine Transdermal System recalls 113,943 cartons after CGMP deviations. Unapproved raw material prompts recall. Stop use immediately and contact Teva or a healthcare provider for guidance.