METOCLOPRAMIDE ORAL SOLUTION — Class III drug recall D-1831-2015
Terminated recall by VistaPharm, Inc., reported 2015-10-07, distributed in CA, IL, LA, OH, PA, SC. Defective Container: Lids on unit dose cups are not fully qualified.
| Recall number | D-1831-2015 |
|---|---|
| Product type | Drug |
| Classification | Class III |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | VistaPharm, Inc., Largo, FL, United States |
| Recall initiated | 2015-06-26 |
| Classified | 2015-09-28 |
| Reported by FDA | 2015-10-07 |
| Terminated | 2017-02-14 |
| Distributed | CA, IL, LA, OH, PA, SC |
| Quantity | 84,100 cups |
| Reason classes | packaging |
| NDC | 66689-0031-01 |
| Lot numbers | 01/17, 387500 |
Product
METOCLOPRAMIDE ORAL SOLUTION, USP 10 mg/10 mL, 10 mL cups, Rx only. Manufactured by VistaPharm, Inc, Largo, FL. NDC: 66689-031-01.
Reason for recall
Defective Container: Lids on unit dose cups are not fully qualified.
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-1831-2015. 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.