# FDA recall D-1697-2012

> **Ben Venue Laboratories Inc** · Class I · drug recall initiated 2012-06-26.

## 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

## Distribution

Nationwide

## Key facts

- **Recall number:** D-1697-2012
- **Recalling firm:** Ben Venue Laboratories Inc
- **Classification:** Class I
- **Product type:** drug
- **Status:** Terminated
- **Initiation date:** 2012-06-26
- **Report date:** 2012-10-03
- **Termination date:** 2014-02-03

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Bedford, OH, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=D-1697-2012

## Citation

> AI Analytics. FDA recall D-1697-2012. Retrieved 2026-05-25 from https://api.ai-analytics.org/recall/D-1697-2012. Source: US FDA. Licensed CC0.

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*[Dataset catalog](/datasets/) · [FDA recalls dataset](/datasets/fda-recalls) · CC0 1.0*
