FDA Drug recall D-1697-2012
Vecuronium Bromide for Injection, For IV use only, 20 mg per vial, 10 x 10 mg Vials, lyophilized powder per carton, Rx Only, Mfr
- FDA Drug
- Class I
- terminated
- Published 2012-10-03
On 2012-10-03 the FDA classified a Class I recall of 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, citing presence of Particulate Matter.
Read the official FDA Drug notice
| Agency | FDA Drug |
|---|---|
| Recall number | D-1697-2012 |
| Classification | Class I |
| Status | terminated |
| Initiated | 2012-06-26 |
| Published | 2012-10-03 |
| Last updated | 2026-09-13 11:51 UTC |
| Company | Ben Venue Laboratories |
| Distribution | US |
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
Presence of Particulate Matter
Identifiers
| code_info | Lot #2067134 Exp 5/31/2013, NDC 55390-039-10 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:51 UTC. Current status: terminated.
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FDA Drug · Class II · 2012-06-20 · Ben Venue Laboratories
All Ben Venue Laboratories recalls
Source
Official record: https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-1697-2012%22
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