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.
Lack of Assurance of Sterility:Lack of validation data for sanitization cycles
Lack of Assurance of Sterility:Lack of validation data for sanitization cycles
Lack of Assurance of Sterility:Lack of validation data for sanitization cycles
Lack of Assurance of Sterility:Lack of validation data for sanitization cycles
Lack of Assurance of Sterility:Lack of validation data for sanitization cycles
Lack of Assurance of Sterility:Lack of validation data for sanitization cycles
Defective Container: slow leakage under the cap
Lack of Assurance of Sterility:Lack of validation data for sanitization cycles
Lack of Assurance of Sterility:Lack of validation data for sanitization cycles
Lack of Assurance of Sterility:Lack of validation data for sanitization cycles
Lack of Assurance of Sterility:Lack of validation data for sanitization cycles
Lack of Assurance of Sterility:Lack of validation data for sanitization cycles
Lack of Assurance of Sterility:Lack of validation data for sanitization cycles
Marketed Without an Approved NDA/ANDA: FDA analysis found the product to be tainted with sildenafil an ingredient found in a FDA approved product for the treatment of male sexual…
CGMP Deviations
CGMP Deviations: Products not manufactured under current good manufacturing practices.
CGMP Deviations: Products not manufactured under current good manufacturing practices.
CGMP Deviations
CGMP Deviations: Products not manufactured under current good manufacturing practices.
CGMP Deviations
CGMP Deviations: Potential exposure to rodents and rodent activity in the distribution center. Also, due to unusually hot weather, FDA Recalled Products may have been subjected to…
Labeling: Missing Label; customer complaint received that labels were partially or completely peeled off injection vial.
CGMP Deviations: Products not manufactured under current good manufacturing practices.
Subpotent: Out of Specification for Assay Test at the 3-month time point.
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.
Recall Lookup USA keeps the last complete source record available when an official data service is temporarily unavailable. When a source provides only a few fields, we show only those known facts rather than padding the page with generic text.
This database is designed for discovery and reference. It can help you locate a relevant recall record, identify the recalling firm or NHTSA campaign, compare dates and classifications, and follow the official source. It is not a substitute for a VIN-specific NHTSA check, a manufacturer notice, medical advice or instructions issued by the recalling company.
