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Prescription drugs recalled for contamination, potency or labelling.
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1,991 recalls · newest first
Subpotent drug
Subpotent drug
Subpotent drug
Subpotent drug
Lack of Assurance of Sterility: Due to wrinkles in the paper lidding which may breach the seal area.
Non-Sterility: Due to presence of Aspergillus penicillioides.
Non-Sterility: Due to presence of Aspergillus penicillioides.
Lack of Assurance of Sterility: Due to wrinkles in the paper lidding which may breach the seal area.
CGMP Deviations
Product Mix-Up: A bottle containing Voriconazole Tablets 50 mg was labelled and distributed as Aripiprazole Tablets USP 30 mg.
Failed Dissolution Specifications: during 12M LT stability testing OOS low for Stage 3 dissolution at the 24-hour timepoint.
Failed Impurities/Degradation Specifications: This recall is being initiated due to out-of-specification results total impurities.
Labeling: Not Elsewhere Classified.
Microbial contamination of sterile products
Labeling: Not Elsewhere Classified.
Defective container:may contain bottles with incomplete seals
Defective container:may contain bottles with incomplete seals
Defective container:may contain bottles with incomplete seals
Defective container:may contain bottles with incomplete seals
Defective container:may contain bottles with incomplete seals