Methotrexate Tablets
Failed Tablet/Capsule Specifications: Tablets were observed to have an unsmooth surface with two tablets demonstrating illegible tablet identification and scoring.
Class III means the product is unlikely to cause harm but violates FDA labeling or manufacturing rules. These are the recalls you rarely hear about; pharmacies usually just swap the affected lot.
1,716 recalls, newest first.
Failed Tablet/Capsule Specifications: Tablets were observed to have an unsmooth surface with two tablets demonstrating illegible tablet identification and scoring.
Subpotent: Out of Specification result observed for Ketorolac assay levels, below the 90.0-110.0% of label claim.
Superpotent Drug - Higher than expected levels of leuprolide acetate in the constituted product.
Subpotent: Out of Specification result observed for low assay
Incorrect/Undeclared Excipients.
Failed Impurities/Degradation Specifications: Out of Specification results in the repackaged product for impurities at the 12-month time point.
Labeling: Label Error on Declared Strength: The incorrect label on the back of the product packaging.
Defective Container: slow leakage under the cap
Cross contamination with other products
Failed dissolution specifications: below specification results at stability 12-month
Failed Impurities/Degradation Specifications
Labeling: Missing Label; customer complaint received that labels were partially or completely peeled off injection vial.
Subpotent: Out of Specification for Assay Test at the 3-month time point.
Subpotent Drug; sub-potent Bromfenac levels, below the 90.0-110.0% specification range.
Labeling: Incorrect or Missing Lot and/or Exp Date: vials were labeled with the incorrect lot number and expiration date
Labeling: Not Elsewhere Classified - the description, warnings, storage information and instructions for use are either missing or partially printed.
Failed Impurities/Degradation Specifications
Failed Impurities/Degradation Specifications: Out-of-specification results observed for the organic impurities test at 6 months, RT Stability.
Out of Specification result observed in content uniformity testing
Superpotent Drug: Out of Specification (OOS) results observed for unit dose content.
Subpotent Drug: Out-of-Specification test results observed in assay test at 21-month long term stability study.
Failed Stability Specifications
Failed Impurities/Degradation Specifications: Out of specification results obtained for conductivity.
Failed Impurities/Degradation Specifications: Out of specification results obtained for conductivity.
Labeling: Label Mix-up