Mycophenolate Mofetil for Oral Suspension — Class III drug recall D-0093-2024
Terminated recall by VistaPharm LLC, reported 2023-11-15, distributed nationwide. Defective Container: The adaptor does not fit into the neck of the bottle after reconstitution with water.
| Recall number | D-0093-2024 |
|---|---|
| Product type | Drug |
| Classification | Class III |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | VistaPharm LLC, Largo, FL, United States |
| Recall initiated | 2023-10-26 |
| Classified | 2023-11-08 |
| Reported by FDA | 2023-11-15 |
| Terminated | 2025-03-21 |
| Distributed | Nationwide (US) |
| Countries outside the US | SA |
| Quantity | 11,633 bottles |
| Reason classes | packaging |
| NDC | 66689-0307, 66689-0307-08 |
| Lot numbers | M23400A, M23401A, M23402A, M23591A, M23592A |
| Expiration dates | 2025-04-30, 2025-06-30 |
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.
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/D-0093-2024. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.