# FDA recall D-0093-2024

> **VistaPharm LLC** · Class III · drug recall initiated 2023-10-26.

## Product

Mycophenolate Mofetil for Oral Suspension, USP, 200 mg/mL, Rx Only, bottle, Manufactured for: VistaPharm, Inc., Largo, FL 33771, USA, NDC#66689-307-08.

## Reason for recall

Defective Container: The adaptor does not fit into the neck of the bottle after reconstitution with water.

## Distribution

Nationwide and Saudi Arabia

## Key facts

- **Recall number:** D-0093-2024
- **Recalling firm:** VistaPharm LLC
- **Classification:** Class III
- **Product type:** drug
- **Status:** Terminated
- **Initiation date:** 2023-10-26
- **Report date:** 2023-11-15
- **Termination date:** 2025-03-21

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Largo, FL, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=D-0093-2024

## Citation

> AI Analytics. FDA recall D-0093-2024. Retrieved 2026-07-20 from https://api.ai-analytics.org/recall/D-0093-2024. Source: US FDA. Licensed CC0.

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