# FDA recall D-1542-2022

> **Viatris Inc** · Class II · drug recall initiated 2022-09-21.

## Product

Ampicillin for Injection, USP, 2 grams/vial NDC 67457-352-02, packaged in 10 x 2 g vials per carton NDC 67457-352-10, Rx only, Mylan Manufactured in India for: Mylan Institutional LLC Rockford, IL 61103 U.S.A

## Reason for recall

Presence of Particulate Matter: A complaint was received for the presence of a single strand of hair in one vial.

## Distribution

Nationwide in the USA

## Key facts

- **Recall number:** D-1542-2022
- **Recalling firm:** Viatris Inc
- **Classification:** Class II
- **Product type:** drug
- **Status:** Terminated
- **Initiation date:** 2022-09-21
- **Report date:** 2022-10-05
- **Termination date:** 2023-10-31

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Canonsburg, PA, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=D-1542-2022

## Citation

> AI Analytics. FDA recall D-1542-2022. Retrieved 2026-07-17 from https://api.ai-analytics.org/recall/D-1542-2022. Source: US FDA. Licensed CC0.

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