Famotidine Tablets
Labeling: Label Error on Declared Strength: some cartons labeled and containing 20 mg may have an external label placed on the side of the carton indicating strength as 10 mg.
41 recalls, newest first
Labeling: Label Error on Declared Strength: some cartons labeled and containing 20 mg may have an external label placed on the side of the carton indicating strength as 10 mg.
Labeling: Incorrect or Missing Package Insert
Labeling: Incorrect or Missing Package Insert
Labeling: Incorrect or Missing Package Insert
Labeling: Incorrect or Missing Package Insert
Labeling: Incorrect or Missing Package Insert
Product mixup: one foreign tablet found in product.
Product mix-up: incorrect product was found inside the G-Supress DX product carton.
Labeling: Typographical error on the upper left-hand side of the box and individual patch label that has the incorrect dosage form stating, each tablet contains instead of each adhesive patch contains.
Labeling: Incorrect or Missing Lot and/or Exp Date: Lot code on primary packaging is incorrect.
Labeling; Incorrect NDC number on outer carton of product.
Labeling: Label Mix-up
Labeling: Incorrect or Missing Lot and/or Exp Date: The carton and bottle labels state an expiry date of March 2026; the correct expiration date is February 2025.
Labeling: Not elsewhere classified
Labeling: Incorrect or Missing Lot and/or Exp Date
Mismatching of the embossing on the tablets (T7) with the embossing mentioned in the package insert (ML63) in the distributed bottles.