Methadone Hydrochloride Tablets
Failed Tablet/Capsule Specifications: Illegible product identification for the unit dose configuration only.
52 recalls · Class III, newest first
Failed Tablet/Capsule Specifications: Illegible product identification for the unit dose configuration only.
LABELING: LABEL MIX-UP
LABELING: LABEL MIX-UP
Labeling: Not Elsewhere Classified: Tablets/Capsules imprinted with wrong ID.
Labeling: Not Elsewhere Classified: Tablets/Capsules imprinted with wrong ID.
Labeling: Not Elsewhere Classified: Tablets/Capsules imprinted with wrong ID.
Labeling: Not Elsewhere Classified: Tablets/Capsules imprinted with wrong ID.
Labeling: Not Elsewhere Classified: Tablets/Capsules imprinted with wrong ID.
Labeling: Not Elsewhere Classified: Tablets/Capsules imprinted with wrong ID.
Labeling: Not Elsewhere Classified: Tablets/Capsules imprinted with wrong ID.
Failed Impurities/Degradation Specifications
Labeling: Not Elsewhere Classified - Wrong NDC number
Failed Tablet/Capsule Specifications
Defective Container: Firm received complaints of broken tube at the seal.
Crystallization: Lack of uniformity - a change in texture, chunky, grainy, and small crystal substances inside the bottles.
Crystallization: Lack of uniformity - a change in texture, chunky, grainy, and small crystal substances inside the bottles.
Discoloration
Cross contamination with other products.
Cross contamination with other products.
Labeling: Incorrect or Missing Lot and/or Exp Date. Missing lot number and expiration dates on packets
Subpotent drug: The potency of the active (menthol) was less than the label claim of 4%.
Subpotent drug: The potency of the active (menthol) was less than the label claim of 4%.
Subpotent drug: The potency of the active (menthol) was less than the label claim of 4%.
Subpotent drug: The potency of the active (menthol) was less than the label claim of 4%.
Failed Impurities/Degradation Specifications: The impurity results at 12 months stability testing,did not conform to the specification limit.