💊 Drugs • 11,927 recalls
Dr. Reddy's Laboratories
CGMP Deviations: Customer complaint for the presence of a staple co-mingled with capsules within the bottle.
Teva Pharmaceuticals USA
Subpotent drug: OOS results of Label Claimed Emitted Dose for salmeterol
Teva Pharmaceuticals USA
Subpotent drug: OOS results of Label Claimed Emitted Dose for salmeterol
SUBPOTENT DRUG: Vial contained a liquid substance, instead of the expected powder substance. There was also a lack of full drug effect upon administration.
SSM Health Care St. Louis
Lack of Assurance of Sterility
Failed Dissolution Specifications
Product Mix-up: Incorrect diluent component included in the kit.
Microbial Contamination of Sterile Products: Confirmed sterility failure identified during stability testing at the 12-month time point.
Lack of Assurance of Sterility: Air filter failed post integrity test leading to a lack of sterility assurance.
Labeling: Incorrect Instructions
IntegraDose Compounding Services
Lack of sterility assurance.
New Vitalis Pharmacy LLC
Lack of Assurance of Sterility
Out-of-specification test results obtained for identification testing based on HPTLC analysis.
Out-of-specification test results obtained for identification testing based on HPTLC analysis.
Defective container: Cracked vials leading to lack of sterility assurance
Washington Homeopathic Products
Out-of-specification test results obtained for identification testing based on HPTLC analysis.
Out-of-specification test results obtained for identification testing based on HPTLC analysis.
Failed Impurities/Degradation Specifications; Out of Specification impurity results obtained during routine testing.
IntegraDose Compounding Services
Lack of sterility assurance.
Out-of-specification test results obtained for identification testing based on HPTLC analysis.