💊 Drugs • 11,927 recalls
Alembic Pharmaceuticals Limited
Labeling: Label-mixup
Washington Homeopathic Products
An error occurred where the product was manufactured with Potassium Chloride instead of Potassium Phosphate.
Cross Contamination with Other Product: Product is being recalled due to Trace Amounts of Quetiapine Fumarate
Temperature Abuse
Defective Delivery System: customer complaints concerning the injector pen breaking apart and disintegrating into pieces.
Defective Delivery System: customer complaints concerning the injector pen breaking apart and disintegrating into pieces.
Crystallization: customer complaints for crystallization in finished product.
Crystallization: customer complaints for crystallization in finished product.
Presence of particulate matter.one confirmed customer report of particulate matter within two semi-rigid bottles identified prior to use
Golden State Medical Supply
Failed Impurities/Degradation Specifications: Out of Specification results obtained for unknown impurities during stability testing by manufacturer
Teva Pharmaceuticals USA
Failed Impurity/Degradation Specifications: Out-of-specifications results observed for impurities during stability testing.
Bryant Ranch Prepack, Inc.
Labeling: Label Mix-Up - Prepackaged bottles labeled spironolactone 50 mg may contain spironolactone 25 mg tablets.
Failed Impurities/Degradation Specifications; out of specification for unknown impurity observed during 6 month stability testing
Breckenridge Pharmaceutical
Failed Impurities/Degradation Specifications: Out-of-Specification results obtained for unknown impurities during stability testing.
cGMP deviations: The quantity of active ingredient used for the product lot was inadvertently taken from an ingredient lot from an alternate supplier before that specific lot was formally qualified for use by the manufacturing site.
Labeling: Label Mix-Up - Prepackaged bottles labeled spironolactone 25 mg may contain spironolactone 50 mg tablets.
Labeling: Incorrect or Missing Lot and/or Exp Date
Lack of Assurance of Sterility: customer complaints of loose crimped vial overseals which may result in a non-sterile product.
Failed pH specifications: Out of Specification pH results for 0.9% Sodium Chloride, USP
Dr. Reddy's Laboratories
Failed Dissolution Specifications: Out-of-specification results observed for dissolution during stability testing.