Clearasil Rapid Rescue Deep Treatment Pads (Salicylic Acid 2%) recall — FDA D-1179-2023
Labeling: Label Error on Declared Strength: The incorrect label on the back of the product packaging.
Browse U.S. drug recall enforcement reports from the FDA in a structured, searchable format. Review the recalled product, reason, firm, status, dates, distribution information and FDA classification when available.
10,685 detailed records are currently available in this category.
Labeling: Label Error on Declared Strength: The incorrect label on the back of the product packaging.
Superpotent Drug - Higher than expected levels of leuprolide acetate in the constituted product.
Stability data does not support expiry: Shelf-life of the impacted lots of BD ChloraPrep" Clear 1 mL Applicator cannot be substantiated beyond 12-months although labeled with 36-month…
Subpotent Drug: Product does not contain SPF that is declared on the label.
Subpotent Drug: Product does not contain SPF that is declared on the label.
Lack of Assurance of Sterility
Lack of Assurance of Sterility
Lack of Assurance of Sterility
Lack of Assurance of Sterility
Lack of Assurance of Sterility
Lack of Assurance of Sterility
Lack of Assurance of Sterility
Lack of Assurance of Sterility
Lack of Assurance of Sterility
Crystallization: bottles of Sandimmune Oral Solution were determined to contain crystals.
Lack of Assurance of Sterility
Lack of Assurance of Sterility
Lack of Assurance of Sterility
Lack of Assurance of Sterility
Lack of Assurance of Sterility
Incorrect/Undeclared Excipients.
Subpotent: Out of Specification result observed for low assay
Lack of Assurance of Sterility
Lack of Assurance of Sterility
A drug recall record can include the reason for recall, firm, status, distribution pattern, quantity and FDA classification. This site does not provide medical advice; it organizes public recall information and links users back to official sources.
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