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Class II · ModerateRecall completed

Infuvite Pediatric

Could cause temporary or reversible harm; serious harm is unlikely.

Does this affect you?
Check your lot numberLot #: JX907, Exp. Date 02/2021
Where it was soldNationwide within the United States
Find the lot number printed on your box or bottle. If it matches — and you take this medicine — call your pharmacist. Don't stop a prescribed medicine on your own.

What happened

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

What to do

  1. Check the lot number and expiry on your medicine against the recall above.
  2. Talk to your pharmacist or doctor before changing anything — don't stop on your own.
  3. Report any problems to FDA MedWatch (1-800-FDA-1088 or fda.gov/medwatch).

Who makes it

Made bySandoz Inc
Brand nameINFUVITE PEDIATRIC
Generic nameMULTIPLE VITAMINS INJECTION
Distributed by / forBaxter Healthcare Corporation Clintec Nutrition Division Deerfield, IL 60015 USA
NDC54643-5647-0
Show the full FDA record
Full product labelInfuvite 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 firmSandoz, Inc
DistributionNationwide within the United States
Quantity17,500 units
Recall initiated2020-04-21
Report date2020-05-13
Recall completed2023-09-07
Recall numberD-1259-2020
ClassificationClass II
FDA statusTerminated
Origin on filePrinceton NJ United States

Related

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Source: U.S. FDA enforcement database (openFDA). Look this up on the official FDA recalls site ↗

This is public FDA recall information, not medical advice. A recall does not always mean your specific bottle is affected. Never stop a prescribed medicine without asking your pharmacist or doctor.