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.
Failed Dissolution Specification: During analysis of the 18 month long term stability testing, it was noticed that the drug release results at the 4 hour time point are not meeting…
Labeling: Incorrect Or Missing Package Insert: Product is labeled with unapproved labeling.
Presence of Particulate Matter
CGMP Deviations: An FDA inspection identified inadequate investigations of past market complaints.
CGMP Deviations: An FDA inspection identified inadequate investigations of past market complaints.
Presence of Particulate Matter: Customer complaint for an insect found free floating inside a single bag for each lot recalled.
Marketed Without An Approved NDA/ANDA: Product was found to contain undeclared diclofenac, a prescription non-steroidal anti-inflammatory drug, and chlorpheniramine, an over-the-counter…
Presence of Foreign Substance: Fragments of wood found when the product was extruded onto a toothbrush.
Incorrect Expiration Date: The "11/06" expiration date printed on the tray (secondary packaging) is incorrect (it should be 11/2016)
Presence of Particulate Matter
Presence of Foreign Substance: Fragments of wood found when the product was extruded onto a toothbrush.
Presence of Foreign Substance: Fragments of wood found when the product was extruded onto a toothbrush.
Presence of Foreign Substance: Fragments of wood found when the product was extruded onto a toothbrush.
Presence of Foreign Substance: Fragments of wood found when the product was extruded onto a toothbrush.
Presence of Foreign Substance: Fragments of wood found when the product was extruded onto a toothbrush.
Presence of Foreign Substance: Fragments of wood found when the product was extruded onto a toothbrush.
Presence of Particulate Matter and Lack of Assurance of Sterility: The firm received a complaint for customer of presence of particulate matter, leaky containers, and missing port…
Presence of Particulate Matter
Presence of Foreign Substance: Fragments of wood found when the product was extruded onto a toothbrush.
Lack of Assurance of Sterility: Due to lack of documentation of proper environmental monitoring during the time in which the medication was produced.
Lack of Assurance of Sterility: Due to lack of documentation of proper environmental monitoring during the time in which the medication was produced.
Lack of Assurance of Sterility: Due to lack of documentation of proper environmental monitoring during the time in which the medication was produced.
Lack of Assurance of Sterility: Due to lack of documentation of proper environmental monitoring during the time in which the medication was produced.
Tablets/Capsules Imprinted with Wrong ID: Some tablets incorrectly imprinted with an X on one side.
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.
