Infuvite PEDiatric Pharmacy — Class II drug recall D-1259-2020
Terminated recall by Sandoz, Inc, reported 2020-05-13, distributed nationwide. Defective Container: Sub-optimal crimping in vial of Pediatric Infuvite Multiple Vitamins
| Recall number | D-1259-2020 |
|---|---|
| Product type | Drug |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Sandoz, Inc, Princeton, NJ, United States |
| Recall initiated | 2020-04-21 |
| Classified | 2020-05-01 |
| Reported by FDA | 2020-05-13 |
| Terminated | 2023-09-07 |
| Distributed | Nationwide (US) |
| Quantity | 17,500 units |
| Reason classes | packaging |
| NDC | 54643-5646, 54643-5646-01, 54643-5647, 54643-5647-00, 54643-5648-01, 54643-5651-01, 54643-5653-00, 54643-5655-00 |
| Lot numbers | JX907 |
| Expiration dates | 2021-02 |
Product
Infuvite PEDiatric Pharmacy, kit in 1 carton (40 mL fill in a 50 mL) vial 1 and (10 mL) in vial 2, Rx Only, Distributed by: Baxter Healthcare Corporation Clintec Nutrition Division Deerfield, IL 60015 USA, NDC 54643-5647-0
Reason for recall
Defective Container: Sub-optimal crimping in vial of Pediatric Infuvite Multiple Vitamins
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-1259-2020. 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.