Data Foundry

Drug recalls 2025

Infuvite Adult — Class II drug recall D-0401-2025

Ongoing recall by Mckesson Medical-Surgical Inc. Corporate Office, reported 2025-05-07, distributed in FL, MS. Severe thunderstorms caused transit delays of certain cold chain products that were shipped on 02-Apr-2025 and

Recall numberD-0401-2025
Product typeDrug
ClassificationClass II
StatusOngoing
Voluntary or mandatedVoluntary
Recalling firmMckesson Medical-Surgical Inc. Corporate Office, Richmond, VA, United States
Recall initiated2025-04-25
Classified2025-05-01
Reported by FDA2025-05-07
DistributedFL, MS
Quantity15
Reason classeslabeling, potency
NDC54643-5649, 54643-5649-01, 54643-5650, 54643-5650-02, 54643-5657-01, 54643-5659-01, 54643-5661-02, 54643-5663-02
Lot numbersAA2279, AA2383
Expiration dates2026-08-31, 2026-09-30

Product

Infuvite Adult, multiple vitamins injection, Baxter, Five of Vial 1 (5 mL) and Five of Vial 2 (5mL), Rx Only, Sterile, Manufactured for: Sandoz Inc., Princeton, NJ 08540, Distributed by Baxter Healthcare Corporation, Deerfield, IL 60015 USA, Product of Canada, NDC 54643-5649-1

Reason for recall

Severe thunderstorms caused transit delays of certain cold chain products that were shipped on 02-Apr-2025 and delivered after the 48-hours specified delivery time, on 07-Apr-2025 and 08-Apr-2025. The affected products may not have been stored at the recommended labeled storage conditions which may have impacted the safety, quality, identity, potency and purity of the product.

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-0401-2025. 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.