17,898 recalls, newest first
Reason Lack of assurance of sterility: Upon review of recent 3rd party environmental certification documentation, it was determined that airflow patterns…
Reason Presence of Foreign Tablets/Capsules: One foreign tablet identified as Clopidogrel 75 mg was found in a 100 count bottle of Metoprolol Succiante…
Reason Failed Dissolution Specifications. High dissolution results were obtained during stability testing.
Reason Failed Dissolution Specifications. High dissolution results were obtained during stability testing.
Reason Failed Dissolution Specifications. High dissolution results were obtained during stability testing.
Reason Labeling: Label Mix-Up: bottle labeled as Diclofenac Sodium and Misoprostol 75 mg/0.2 mg contained Diclofenac Sodium and Misoprostol 50 mg/0.2 mg…
Reason Presence of Foreign Substance:Sun Pharma is recalling one (1) lot of Sulfamethoxazole and Trimethoprim Tablets USP, 800 mg/160 mg (500 ct.) because…
Reason Failed Dissolution Specification: Low dissolution outside of specifications
Reason Marketed Without An Approved NDA/ANDA: product contains undeclared sildenafil, tadalafil, and oxytetracycline, FDA approved drug products making…
Reason Failed Impurities/Degradation: This recall has been initiated due to an out of specification (OOS) result that was obtained for related substance…
Reason Labeling: Labeling Error on Declared Strength; The outer carton (secondary packaging) statement of ingredients misstates the concentration of active…
Reason Subpotent Drug
Reason Subpotent Drug
Reason Subpotent Drug
Reason Marketed Without An Approved NDA/ANDA: FDA analysis found the product to contain undeclared tadalafil. The presence of tadalafil makes Rhino Extreme…
Reason Lack of Assurance of Sterility:Microbial contamination was detected during routine testing of subsequent unreleased product lots due to interaction…
Reason Lack of Assurance of Sterility:Microbial contamination was detected during routine testing of subsequent unreleased product lots due to interaction…
Reason Lack of Assurance of Sterility:Microbial contamination was detected during routine testing of subsequent unreleased product lots due to interaction…
Reason Lack of Assurance of Sterility:Microbial contamination was detected during routine testing of subsequent unreleased product lots due to interaction…
Reason Failed Stability Specifications
Reason Presence of Foreign Tablets/Capsules
Reason cGMP deviations
Reason Subpotent drug: Out of specification for an active ingredient cysteamine hydrochloride.
Reason Defective Delivery System: Out of specification for adhesive transfer.
Reason Cross Contamination With Other Products: presence of unrelated ingredients (i.e. traces of Lisinopril, Mannitol, Iron, Calcium and Phosphorous).