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.
Recalled products were made using an active ingredient that was recalled by a supplier due to penicillin cross contamination.
Presence of Foreign Tablets/Capsules: one foreign capsule identified as omeprazole 10 mg was found in the bottle
Recalled products were made using an active ingredient that was recalled by a supplier due to penicillin cross contamination.
Recalled products were made using an active ingredient that was recalled by a supplier due to penicillin cross contamination.
Recalled products were made using an active ingredient that was recalled by a supplier due to penicillin cross contamination.
Recalled products were made using an active ingredient that was recalled by a supplier due to penicillin cross contamination.
Recalled products were made using an active ingredient that was recalled by a supplier due to penicillin cross contamination.
Recalled products were made using an active ingredient that was recalled by a supplier due to penicillin cross contamination.
Recalled products were made using an active ingredient that was recalled by a supplier due to penicillin cross contamination.
Recalled products were made using an active ingredient that was recalled by a supplier due to penicillin cross contamination.
Recalled products were made using an active ingredient that was recalled by a supplier due to penicillin cross contamination.
Recalled products were made using an active ingredient that was recalled by a supplier due to penicillin cross contamination.
Recalled products were made using an active ingredient that was recalled by a supplier due to penicillin cross contamination.
Marketed Without An Approved NDA/ANDA: Miracle Diet 30 was found to contain undeclared phenolphthalein, a drug product once contained in over-the-counter laxatives but was taken off the…
Labeling: Wrong Bar Code
Recalled products were made using an active ingredient that was recalled by a supplier due to penicillin cross contamination.
Recalled products were made using an active ingredient that was recalled by a supplier due to penicillin cross contamination.
Recalled products were made using an active ingredient that was recalled by a supplier due to penicillin cross contamination.
Recalled products were made using an active ingredient that was recalled by a supplier due to penicillin cross contamination.
Recalled products were made using an active ingredient that was recalled by a supplier due to penicillin cross contamination.
Recalled products were made using an active ingredient that was recalled by a supplier due to penicillin cross contamination.
Marketed Without An Approved NDA/ANDA: Miracle Rock 48 was found to contain undeclared thiosildenafil, an analogue of an FDA approved drug for male erectile dysfunchtion making this product…
Recalled products were made using an active ingredient that was recalled by a supplier due to penicillin cross contamination.
Recalled products were made using an active ingredient that was recalled by a supplier due to penicillin cross contamination.
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.
