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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

Medroxyprogesterone and Infuvite Injections Recalled for Temperature Exposure

Agency Publication Date: May 1, 2025
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Summary

Mckesson Medical-Surgical Inc. has recalled 18 units of Medroxyprogesterone Acetate (medroxyprogesterone) and Infuvite Adult (multiple vitamins) injections. These cold chain products were shipped on April 2, 2025, but were delayed by severe thunderstorms and delivered five to six days later, exceeding the required 48-hour delivery window. Because the products were not kept at the recommended cold temperatures during this delay, their safety, quality, and effectiveness may be compromised.

Risk

The affected medications may not have been stored at the required temperatures, which can impact the medicine's potency, purity, and safety. Using compromised injectable medications could result in less effective treatment or other health risks.

What You Should Do

  1. This recall affects Medroxyprogesterone Acetate Injectable Suspension (NDC 55150-0330-01) lot 1MP24042, and Infuvite Adult multiple vitamins injection (NDC 54643-5649-1) lots AA2279 and AA2383.
  2. Stop using the recalled product immediately.
  3. Contact Mckesson Medical-Surgical Inc. or your distributor to arrange for the return of any remaining affected units.
  4. Call the FDA Consumer Complaint hotline at 1-888-723-3332 for more information.

Your Remedy Options

๐Ÿ“‹Other Action
How to: Stop using the recalled product. Contact the manufacturer or your distributor to arrange return.

Affected Products

Product: Medroxyprogesterone Acetate Injectable Suspension, USPby Eugia
Variants: 150 mg / mL, 1 mL Single-Dose Vial
Lot Numbers:
1MP24042 (Exp 6/30/26)
NDC:
55150-0330-01

Manufactured for Eugia US LLC.

Product: Infuvite Adult, multiple vitamins injectionby Baxter
Variants: Five of Vial 1 (5 mL) and Five of Vial 2 (5 mL)
Lot Numbers:
AA2279 (Exp 8/31/26)
AA2383 (Exp 9/30/26)
NDC:
54643-5649-1

Manufactured for Sandoz Inc.; Distributed by Baxter Healthcare Corporation.

Additional Information

Agency: Food and Drug Administration (FDA)
Event ID: 96744
Status: Active
Manufacturer: Mckesson Medical-Surgical Inc. Corporate Office
Sold By: Medical Facilities
Manufactured In: India, Canada
Units Affected: 2 products (3; 15)
Distributed To: Mississippi, Florida

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 ยท 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.