Sabril — Class III drug recall D-1142-2023
Completed recall by Lundbeck LLC, reported 2023-09-06, distributed nationwide. Cross contamination with other products
| Recall number | D-1142-2023 |
|---|---|
| Product type | Drug |
| Classification | Class III |
| Status | Completed |
| Voluntary or mandated | Voluntary |
| Recalling firm | Lundbeck LLC, Deerfield, IL, United States |
| Recall initiated | 2023-08-17 |
| Classified | 2023-08-29 |
| Reported by FDA | 2023-09-06 |
| Distributed | Nationwide (US) |
| Quantity | 10,543 cartons |
| NDC | 67386-0211, 67386-0211-65 |
| Lot numbers | 3207333A, 3207334A, 3214707A, 3214709A, 3214710A |
| Expiration dates | 2027-03, 2028-02 |
Product
Sabril (vigabatrin) for Oral Solution, 500 mg, 50 Packets, Rx only, Manufactured by: Patheon, Cincinnati, OH 45237, NDC 67386-211-65
Reason for recall
Cross contamination with other products
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/D-1142-2023. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.