Vecuronium Bromide for Injection 20 mg* *1mg/mL when reconstituted to… — Class I drug recall D-0373-2019
Terminated recall by Sun Pharmaceutical Industries, Inc., reported 2019-01-16, distributed nationwide. Presence of Particulate Matter: Foreign matter identified as glass detected in Vecuronium Bromide for Injectio
| Recall number | D-0373-2019 |
|---|---|
| Product type | Drug |
| Classification | Class I |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Sun Pharmaceutical Industries, Inc., Cranbury, NJ, United States |
| Recall initiated | 2019-01-03 |
| Classified | 2019-01-14 |
| Reported by FDA | 2019-01-16 |
| Terminated | 2021-11-03 |
| Distributed | Nationwide (US) |
| Reason classes | foreign material, specification failure |
| NDC | 47335-0931, 47335-0931-40, 47335-0931-44, 47335-0932, 47335-0932-40, 47335-0932-44 |
| Lot numbers | JKS0400A |
| Expiration dates | 2019-03 |
Product
Vecuronium Bromide for Injection 20 mg* *1mg/mL when reconstituted to 20 mL Lyophilized, 10 x 20 mg vials, Rx Only, Manufactured by: Sun Pharmaceutical Industries Ltd. Halol-Baroda Highway Halol-389 350, Gujarat, India. Distributed by: Sun Pharmaceutical Industries, Inc. Cranbury, NJ 08512 NDC: 47335-932-40 [vial] 47335-932-44 [carton]
Reason for recall
Presence of Particulate Matter: Foreign matter identified as glass detected in Vecuronium Bromide for Injection.
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-0373-2019. 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.