Browse Drug Recalls
9 FDA drug safety recalls.
FDA Drug Recall Enforcement Database
Browse 9 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 9 FDA drug recalls.
| Date | Product | Reason | Class | Firm |
|---|---|---|---|---|
| Jan 10, 2014 | Dermamedics Calm and Correct Serum, 2 oz. containers with a SKU number of BB1... | Marketed without an Approved NDA/ANDA: FDA has determined that the products are unapproved new dr... | Class II | Dermamedics, L.L.C. |
| Jan 10, 2014 | Dermamedics Post Procedure Cream 1 oz. containers in the Dermamedics Post-Las... | Marketed without an Approved NDA/ANDA: FDA has determined that the products are unapproved new dr... | Class II | Dermamedics, L.L.C. |
| Jan 10, 2014 | Dermamedics Complexion Repair Topical Rehydrating Emulsion in 50 ml and 30 ml... | Marketed without an Approved NDA/ANDA: FDA has determined that the products are unapproved new dr... | Class II | Dermamedics, L.L.C. |
| Jan 10, 2014 | Dermamedics Calm & Correct Cream in 2 oz. containers with SKU number DM1020. | Marketed without an Approved NDA/ANDA: FDA has determined that the products are unapproved new dr... | Class II | Dermamedics, L.L.C. |
| Jan 10, 2014 | Therametics Complexion Repair Topical Rehydrating Emulsion in 50 ml and 30 ml... | Marketed without an Approved NDA/ANDA: FDA has determined that the products are unapproved new dr... | Class II | Dermamedics, L.L.C. |
| Jan 10, 2014 | Dermamedics Baby's Relief Calm and Repair Cream in 2 oz. containers with a SK... | Marketed without an Approved NDA/ANDA: FDA has determined that the products are unapproved new dr... | Class II | Dermamedics, L.L.C. |
| Jan 10, 2014 | Dermamedics Calm and Correct Cream 2 oz. containers in the Dermamedics Post M... | Marketed without an Approved NDA/ANDA: FDA has determined that the products are unapproved new dr... | Class II | Dermamedics, L.L.C. |
| Jan 10, 2014 | Dermamedics Complexion Repair Topical Rehydrating Emulsion which was distribu... | Marketed without an Approved NDA/ANDA: FDA has determined that the products are unapproved new dr... | Class II | Dermamedics, L.L.C. |
| Jan 10, 2014 | Dermamedics Post Procedure Cream, 1 ounce containers which were distributed w... | Marketed without an Approved NDA/ANDA: FDA has determined that the products are unapproved new dr... | Class II | Dermamedics, L.L.C. |
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.