# FDA recall D-0734-2026

> **MYLAN PHARMACEUTICALS INC** · Class II · drug recall initiated 2026-07-02.

## Product

Mycophenolate Mofetil for Injection USP, 500 mg/Vial, Single Dose Vial, 4 vials per carton, Rx only, Manufactured for: Mylan Institutional LLC, Morgantown, WV, 26505 USA, Made in India, NDC 67457-386-00 (vial label) & NDC 67457-386-81 (carton label).

## Reason for recall

Presence of precipitate

## Distribution

USA Nationwide

## Key facts

- **Recall number:** D-0734-2026
- **Recalling firm:** MYLAN PHARMACEUTICALS INC
- **Classification:** Class II
- **Product type:** drug
- **Status:** Ongoing
- **Initiation date:** 2026-07-02
- **Report date:** 2026-08-05

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Morgantown, WV, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=D-0734-2026

## Citation

> AI Analytics. FDA recall D-0734-2026. Retrieved 2026-09-01 from https://api.ai-analytics.org/recall/D-0734-2026. Source: US FDA. Licensed CC0.

---

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