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Recalls

More Than 2.5 Million Lupin Eye Drop Bottles Recalled Nationwide

The FDA classified the action as Class II because a possible foreign substance was found, requiring patients to stop using affected bottles.

FDA Classifies Chlorthalidone Recall as Class II

Nationwide Recall of 25 mg Chlorthalidone Covers 11,460 Bottles

More Than 370,000 Duloxetine Bottles Recalled Over Nitrosamine Contamination

Viatris Recalls One Lot of Xanax XR Nationwide After Tablets Fail FDA Dissolution Test

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

FDA Class III Recall Targets 11,136 Bottles of Ziac Over Trace Ezetimibe Contamination

FDA Class II Recall Issued for 141,984 Bottles of Generic Atorvastatin Over Dissolution Failures

FDA Class II Recall Targets 580,000 Prazosin Bottles for Nitrosamine Overages