# FDA recall D-1293-2019

> **Par Pharmaceutical, Inc.** · Class I · drug recall initiated 2019-04-30.

## Product

Mycophenolate Mofetil for Injection, USP  500 mg, 4 Single Dose Vials, Rx Only, Distributed by: Par Pharmaceutical Chestnut Ridge, NY 10977  NDC 342023-172-044

## Reason for recall

Presence of Particulate Matter; glass fragment observed in one vial of reconstituted product

## Distribution

nationwide

## Key facts

- **Recall number:** D-1293-2019
- **Recalling firm:** Par Pharmaceutical, Inc.
- **Classification:** Class I
- **Product type:** drug
- **Status:** Terminated
- **Initiation date:** 2019-04-30
- **Report date:** 2019-05-15
- **Termination date:** 2023-06-20

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Chestnut Ridge, NY, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=D-1293-2019

## Citation

> AI Analytics. FDA recall D-1293-2019. Retrieved 2026-07-19 from https://api.ai-analytics.org/recall/D-1293-2019. Source: US FDA. Licensed CC0.

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