FDAFDA · Food and drugs·Recall number D-0401-2025
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
Published May 7, 2025 · Recall initiated: April 25, 2025
Status when published: Ongoing — openFDA updates weekly, so this field may not reflect the current status. Always confirm with the official notice.
What's the hazard
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.
What to do
Voluntary: Firm initiated
Recall details
- Brand
- INFUVITE ADULT
- Manufacturer
- Mckesson Medical-Surgical Inc. Corporate Office
- Distributor
- Distributed to Medical Facilities in MS and FL.
- Lot
- Lot #: AA2279, Exp 8/31/26; AA2383, Exp 9/30/26
- Risk classification
- Class II
- Area (FDA)
- drug
- Country
- United States
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