FDA Drug recall D-0590-2021
VIMPAT (lacosamide) Tablets, 200mg, 60-count bottle, Rx Only, Manufactured for: UCB, Inc
- FDA Drug
- Class II
- terminated
- Published 2021-06-02
On 2021-06-02 the FDA classified a Class II recall of VIMPAT (lacosamide) Tablets, 200mg, 60-count bottle, Rx Only, Manufactured for: UCB, Inc by Cardinal Health, citing CGMP Deviations: Intermittent exposure to temperature excursion during storage.
Read the official FDA Drug notice
| Agency | FDA Drug |
|---|---|
| Recall number | D-0590-2021 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2021-03-15 |
| Published | 2021-06-02 |
| Last updated | 2026-09-13 11:52 UTC |
| Company | Cardinal Health |
| Distribution | FL, GA, SC |
Product
VIMPAT (lacosamide) Tablets, 200mg, 60-count bottle, Rx Only, Manufactured for: UCB, Inc. Smyrna, GA 30080, NDC 0131-2480-35
Reason
CGMP Deviations: Intermittent exposure to temperature excursion during storage.
Identifiers
| ndc | 0131-2477-35 |
|---|---|
| ndc | 0131-2477-60 |
| ndc | 0131-2477-99 |
| ndc | 0131-2478-35 |
| ndc | 0131-2478-60 |
| ndc | 0131-2478-99 |
| ndc | 0131-2479-35 |
| ndc | 0131-2479-60 |
| ndc | 0131-2479-99 |
| ndc | 0131-2480-35 |
| ndc | 0131-2480-60 |
| ndc | 0131-2480-99 |
| ndc | 0131-1810-67 |
| ndc | 0131-5410-70 |
| ndc | 0131-5410-71 |
| ndc | 0131-5410-72 |
| code_info | 912064 |
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:52 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-0590-2021%22
RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.