# FDA recall D-1369-2012

> **Meridian Medical Technologies a Pfizer Company** · Class II · drug recall initiated 2012-06-06.

## Product

Diazepam Injection, USP, 10 mg Automatic, Autoinjector for Buddy Use, 5 mg/mL, 2 mL autoinjector, 15-count autoinjectors per carton, Rx only, Meridian Medical Technologies, Columbia, MD  21046; A subsidiary of King Pharmaceuticals, Inc.; NSN 6505-01-274-0951, NDC 11704-600-01.

## Reason for recall

Impurities/Degradation Products: High Out of Specification levels for carbostyril, a known degradation product of diazepam.

## Distribution

Nationwide, military, Italy, Singapore, Sweden, and Canada.

## Key facts

- **Recall number:** D-1369-2012
- **Recalling firm:** Meridian Medical Technologies a Pfizer Company
- **Classification:** Class II
- **Product type:** drug
- **Status:** Terminated
- **Initiation date:** 2012-06-06
- **Report date:** 2012-06-20
- **Termination date:** 2013-08-05

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Saint Louis, MO, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=D-1369-2012

## Citation

> AI Analytics. FDA recall D-1369-2012. Retrieved 2026-05-25 from https://api.ai-analytics.org/recall/D-1369-2012. Source: US FDA. Licensed CC0.

---

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