Browse Drug Recalls
7 FDA drug safety recalls.
FDA Drug Recall Enforcement Database
Browse 7 FDA drug recall enforcement actions. Each entry includes the product description, reason for recall, classification (Class I through III based on severity), recalling firm, and distribution details. Use the filters below to search by year, classification, state, or keyword.
Drug Safety Recalls
Browse 7 FDA drug recalls.
| Date | Product | Reason | Class | Firm |
|---|---|---|---|---|
| Feb 16, 2022 | Sure Regular Antiperspirant Deodorant Aerosol (Aluminum Chlorohydrate 10%), p... | Chemical contamination: Presence of benzene | Class I | TCP HRB ACQUISITON LLC |
| Feb 16, 2022 | Brut Classic Antiperspirant & Deodorant (aluminum chlorohydrate 20.9%) packag... | Chemical contamination: Presence of benzene | Class I | TCP HRB ACQUISITON LLC |
| Feb 16, 2022 | Sure Unscented Anti-perspirant Deodorant Aerosol (Aluminum Chlorohydrate 10%)... | Chemical contamination: Presence of benzene | Class I | TCP HRB ACQUISITON LLC |
| Nov 20, 2019 | SURE 48hr Confidence Unscented Original Solid Anti-Perspirant & Deodorant Net... | Labeling Product Contains Undeclared API: Active Ingredient on label is not the active ingredient... | Class III | Idelle Labs |
| Nov 20, 2019 | SURE 48hr Confidence Nourishing Coconut invisible solid Antiperspirant & Deod... | Labeling Product Contains Undeclared API: Active Ingredient on label is not the active ingredient... | Class III | Idelle Labs |
| Nov 20, 2019 | SURE 48hr Confidence Regular Original Solid Anti-Perspirant & Deodorant Net W... | Labeling Product Contains Undeclared API: Active Ingredient on label is not the active ingredient... | Class III | Idelle Labs |
| Nov 20, 2019 | SURE 48 hr Confidence Unscented invisible solid Anti-Perspirant & Deodorant, ... | Labeling Product Contains Undeclared API: Active Ingredient on label is not the active ingredient... | Class III | Idelle Labs |
Frequently Asked Questions
When a drug safety issue is identified — through FDA inspections, laboratory testing, adverse event reports, or manufacturer quality checks — the responsible company issues a recall to remove the affected products from the market. Pharmacies pull the product from shelves, and consumers are advised to contact their healthcare provider for alternatives.
The leading causes include cGMP deviations, impurity contamination (including nitrosamines like NDMA), failed dissolution or stability testing, sterility issues, potency problems, labeling errors, and foreign particle contamination.
Use the search and filter tools on this page to look up specific medications, active ingredients, or manufacturers. Each recall entry includes the product description, lot numbers, and distribution details.