# FDA recall D-0373-2024

> **Mckesson Medical-Surgical Inc. Corporate Office** · Class II · drug recall initiated 2024-02-07.

## Product

Bicillin L-A (Penicillin G Benzathine) 1.2, MMU / 2 mL Injection Prefilled Syringe 2 mL, Rx only, Mfg: Pfizer Pharmaceuticals, NDC 60793-0701-10

## Reason for recall

cGMP Deviations: Products were stored outside the drug label specifications.

## Distribution

Product was distributed to three direct accounts in NM, AZ and UT.

## Key facts

- **Recall number:** D-0373-2024
- **Recalling firm:** Mckesson Medical-Surgical Inc. Corporate Office
- **Classification:** Class II
- **Product type:** drug
- **Status:** Terminated
- **Initiation date:** 2024-02-07
- **Report date:** 2024-03-20
- **Termination date:** 2024-08-14

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Richmond, VA, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=D-0373-2024

## Citation

> AI Analytics. FDA recall D-0373-2024. Retrieved 2026-06-26 from https://api.ai-analytics.org/recall/D-0373-2024. Source: US FDA. Licensed CC0.

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