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FDA Lists Nine Eye-Care Products in Recall Over Sterility Concerns

The manufacturer initiated the action that the FDA classified as Class II, prompting consumers to check lot numbers and stop using matched products.

Anvisa Orders Recall of Paramol 750 mg Lot After Tablets Show Mold-Like Spots

Anvisa Suspends Import of Excelvision Eye Medicines

Anvisa Seizes Falsified Mounjaro Lots and Bans Unregistered Supplements

FDA Upgrades Children’s Ibuprofen Recall to Class II Over Reports of Foreign Material

Systane Eye Drops Recalled Over Potential Fungal Contamination

US Drug Shortages Reach Record Highs