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.
10,690 detailed records are currently available in this category.
Defective Container: Excess lidding material accumulation between the seal and the cup resulting in the lid not properly adhering and allowing leakage.
Labeling: Not elsewhere classified - count on the label was incorrect.
Labeling: Incorrect or Missing Lot and/or Exp Date: Potential for the lot number and/or expiration date to be faded or missing from the primary label on the glass vial.
Chemical Contamination: Potential for contamination of the products with an aromatic hydrocarbon resin.
Chemical Contamination: Potential for contamination of the products with an aromatic hydrocarbon resin.
Chemical Contamination: Potential for contamination of the products with an aromatic hydrocarbon resin.
Chemical Contamination: Potential for contamination of the products with an aromatic hydrocarbon resin.
Presence of Foreign Substance: Product complaint for the presence of foreign matter identified as silicone within the tablet.
Incorrect/ Undeclared Excipient: Firm is recalling product due to an incorrect statement of Preservative free on the individual carton label. The vial label and outer carton label contain…
Labeling: Incorrect or Missing Lot and/or Exp Date
Labeling: Incorrect or Missing Lot and/or Exp Date
Failed Impurities/Degradation Specifications: Out of specification for impurities.
Failed Impurities/Degradation Specifications: Out of specification for impurities.
Lack of Assurance of Sterility: incomplete or missing data regarding production.
Lack of Assurance of Sterility: incomplete or missing data regarding production.
Failed Impurities/Degradation Specifications: Out of specification for impurities.
Lack of Assurance of Sterility: incomplete or missing data regarding production.
Defective Delivery System: Product may contain leaking capsules.
Failed Impurities/Degradation Specifications: Out of specification for impurities.
Failed Impurities/Degradation Specifications: Product recalled due to elevated impurity result detected during routine stability testing.
Stability Does Not Support Expiry: manufactured with an active ingredient that expired before the labeled Beyond Use Date.
Stability Does Not Support Expiry: manufactured with an active ingredient that expired before the labeled Beyond Use Date.
Labeling: Incorrect or Missing Lot and/or Exp Date: the individual blisters are mislabeled with an incorrect lot number of 13560 rather than the correct lot number of 13650.
Superpotent Drug: one ingredient was found to be above assay specification.
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.
