Vecuronium Bromide for Injection — Class I drug recall D-1697-2012
Terminated recall by Ben Venue Laboratories Inc, reported 2012-10-03, distributed nationwide. Presence of Particulate Matter
| Recall number | D-1697-2012 |
|---|---|
| Product type | Drug |
| Classification | Class I |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Ben Venue Laboratories Inc, Bedford, OH, United States |
| Recall initiated | 2012-06-26 |
| Classified | 2012-09-26 |
| Reported by FDA | 2012-10-03 |
| Terminated | 2014-02-03 |
| Distributed | Nationwide (US) |
| Reason classes | specification failure |
| NDC | 55390-0039-10 |
| Lot numbers | 2067134 |
| Expiration dates | 2013-05-31 |
Product
Vecuronium Bromide for Injection, For IV use only, 20 mg per vial, 10 x 10 mg Vials, lyophilized powder per carton, Rx Only, Mfr. By: Ben Venue Laboratories, Bedford, OH 44146: Mfg for: Bedford Labs, Bedford, OH 44146, NDC 55390-039-10.
Reason for recall
Presence of Particulate Matter
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-1697-2012. 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.