US Drug Recall Register
Class II · Moderate risk Terminated Initiated Apr 21, 2020 (6 years ago)

Infuvite PEDiatric Pharmacy, kit in 1 carton (40 mL fill in a 50 mL) vial 1 and (10 mL)…

Class II — Moderate risk. May cause temporary or reversible harm; serious harm unlikely.

Why it was recalled

Defective Container: Sub-optimal crimping in vial of Pediatric Infuvite Multiple Vitamins

What was recalled

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

Recalling firm
Sandoz, Inc
NDC code
54643-5647-0
Origin
NJ, United States
Initiated by
Voluntary: Firm initiated
FDA recall number
D-1259-2020

What should you do? A recall doesn't always mean your specific bottle is affected - it often applies to certain lots only. Check the lot number on your package against the FDA notice, and talk to your pharmacist before stopping any medication.