# FDA recall D-0373-2019

> **Sun Pharmaceutical Industries, Inc.** · Class I · drug recall initiated 2019-01-03.

## 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.

## Distribution

Nationwide in the USA

## Key facts

- **Recall number:** D-0373-2019
- **Recalling firm:** Sun Pharmaceutical Industries, Inc.
- **Classification:** Class I
- **Product type:** drug
- **Status:** Terminated
- **Initiation date:** 2019-01-03
- **Report date:** 2019-01-16
- **Termination date:** 2021-11-03

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Cranbury, NJ, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=D-0373-2019

## Citation

> AI Analytics. FDA recall D-0373-2019. Retrieved 2026-06-02 from https://api.ai-analytics.org/recall/D-0373-2019. Source: US FDA. Licensed CC0.

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