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Recall data is sourced from official U.S. government agencies (CPSC, FDA, NHTSA, USDA) and processed using AI to improve readability. This site is not affiliated with or endorsed by any government agency. Always refer to the original agency notice for authoritative information.

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Medium RiskFDA Drug
Medications & Supplements/Prescription Drugs

Sandoz, Inc: Pediatric Infuvite Multiple Vitamins Recalled for Defective Vial Seals

Agency Publication Date: May 1, 2020
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Summary

Sandoz, Inc. is recalling 17,500 units of Infuvite PEDiatric Pharmacy kits due to sub-optimal crimping on the vials. This defect involves the metal ring that secures the stopper to the vial, which may not be properly sealed. The recall affects pharmacy kits containing two vials with 40 mL and 10 mL fills, identified by lot number JX907. Consumers should contact their healthcare provider or pharmacist regarding the use of this medication and for instructions on returning the product.

Risk

A sub-optimal seal or crimp on a medication vial can compromise the sterility of the product or lead to leakage. If the product's sterility is lost, there is a risk of infection or contamination when the vitamins are administered to pediatric patients.

What You Should Do

  1. Check your pharmacy supply or medication kit for Infuvite PEDiatric Pharmacy kits with NDC 54643-5647-0.
  2. Verify the lot number on the packaging; only lot number JX907 with an expiration date of 02/2021 is included in this recall.
  3. Contact your healthcare provider or pharmacist immediately for guidance if you possess the affected product.
  4. Return any unused product from the affected lot to your pharmacy for a refund.
  5. Contact Sandoz, Inc. at 1-888-723-3332 for further instructions regarding this recall.
  6. For additional questions, contact the FDA Consumer Complaint hotline at 1-888-723-3332 (1-888-SAFEFDA) or visit www.fda.gov/safety/recalls.

Your Remedy Options

💰Full Refund

Contact healthcare provider and return product

How to: Contact your healthcare provider or pharmacist for guidance. Return any unused product to the pharmacy for a refund

Affected Products

Product: Infuvite PEDiatric Pharmacy kit (40 mL fill in a 50 mL vial 1 and 10 mL in vial 2)
Model:
NDC 54643-5647-0
Lot Numbers:
JX907 (Exp. 02/2021)
Date Ranges: Expiration Date 02/2021

Additional Information

Agency: Food and Drug Administration (FDA)
Event ID: 85538
Status: Resolved
Manufacturer: Sandoz, Inc
Sold By: Baxter Healthcare Corporation Clintec Nutrition Division
Manufactured In: United States
Units Affected: 17,500 units
Distributed To: Nationwide

Were You Affected by This Recall?

If you or a family member were harmed by this recalled product, you may have legal rights. Consider consulting a consumer protection attorney to understand your options for compensation.

Find an Attorney

This is general information, not legal advice. Go Backs is not a law firm and does not provide legal services.

AI-Enhanced Content: The summary, action steps, and risk assessment on this page were generated by AI from official government recall data to improve readability. This is not legal or medical advice. Always refer to the official agency sources below for authoritative information.

Sources: FDA iRES · Raw API Response

openFDA Disclaimer: This recall information is sourced from the openFDA API. Do not rely on openFDA to make decisions regarding medical care. While we make every effort to ensure that data is accurate, you should assume all results are unvalidated. Refer to the openFDA terms of service for more information.