ONDANSETRON 8 MG / 50 ml NS IVPB — Class II drug recall D-1794-2019
Terminated recall by Infusion Options, Inc., reported 2019-08-21, distributed in NY. Lack of Assurance of Sterility
| Recall number | D-1794-2019 |
|---|---|
| Product type | Drug |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Infusion Options, Inc., Brooklyn, NY, United States |
| Recall initiated | 2019-06-12 |
| Classified | 2019-08-15 |
| Reported by FDA | 2019-08-21 |
| Terminated | 2025-03-21 |
| Distributed | NY |
| Reason classes | sterility |
Product
ONDANSETRON 8 MG / 50 ml NS IVPB, Rx Only, Infusion Options, Inc. 5924 13the Ave, Brooklyn, NY 11219-4934, 718-283-7233
Reason for recall
Lack of Assurance of Sterility
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-1794-2019. 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.