95,114 total recalls in our database
South Coast Specialty Compounding
Penicillin Cross Contamination: Multiple finished products potentially contaminated with penicillin.
Qualitest Pharmaceuticals
Failed Tablet/Capsule Specifications; report of oversized and discolored tablets
South Coast Specialty Compounding
Penicillin Cross Contamination: Multiple finished products potentially contaminated with penicillin.
South Coast Specialty Compounding
Penicillin Cross Contamination: Multiple finished products potentially contaminated with penicillin.
South Coast Specialty Compounding
Penicillin Cross Contamination: Multiple finished products potentially contaminated with penicillin.
South Coast Specialty Compounding
Penicillin Cross Contamination: Multiple finished products potentially contaminated with penicillin.
South Coast Specialty Compounding
Penicillin Cross Contamination: Multiple finished products potentially contaminated with penicillin.
South Coast Specialty Compounding
Penicillin Cross Contamination: Multiple finished products potentially contaminated with penicillin.
South Coast Specialty Compounding
Penicillin Cross Contamination: Multiple finished products potentially contaminated with penicillin.
South Coast Specialty Compounding
Penicillin Cross Contamination: Multiple finished products potentially contaminated with penicillin.
Silarx Pharmaceutical
Labeling: Incorrect or Missing Lot and/or Exp. Date - Firm received a customer complaint that the expiration date printed on the unit carton (5/18) does not match the expiration date on the bottle label (5/17).
Recall initiated due to inadequate validation/qualification of sterilization processes, and package integrity for products released for distribution as sterile.
Recall initiated due to inadequate validation/qualification of sterilization processes, and package integrity for products released for distribution as sterile.
Recall initiated due to inadequate validation/qualification of sterilization processes, and package integrity for products released for distribution as sterile.
Jackscrew nut part failure potentially leading to device malfunction and patient/operator injury.
Recall initiated due to inadequate validation/qualification of sterilization processes, and package integrity for products released for distribution as sterile.
Recall initiated due to inadequate validation/qualification of sterilization processes, and package integrity for products released for distribution as sterile.
Recall initiated due to inadequate validation/qualification of sterilization processes, and package integrity for products released for distribution as sterile.
Recall initiated due to inadequate validation/qualification of sterilization processes, and package integrity for products released for distribution as sterile.
Recall initiated due to inadequate validation/qualification of sterilization processes, and package integrity for products released for distribution as sterile.