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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 Acetate Injection Recalled for Manufacturing Issues

Agency Publication Date: January 6, 2025
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Summary

Eugia US LLC is voluntarily recalling medroxyPROGESTERone Acetate Injectable Suspension, USP (150mg per mL), a prescription hormonal medication. Approximately 19,872 vials are affected by this recall because the manufacturing process did not meet required quality standards (CGMP deviations). No injuries or adverse events have been reported to date, but the company is recalling the lot as a precaution to ensure patient safety.

Risk

Because of deviations from Good Manufacturing Practices, the quality, safety, and purity of this injectable medication cannot be guaranteed. Using a drug that does not meet strict manufacturing standards could result in treatment that is less effective or poses unknown health risks.

What You Should Do

  1. This recall involves medroxyPROGESTERone Acetate Injectable Suspension, USP, 150mg per mL, sold in 1 mL single-dose vials with NDC 55150-329-01.
  2. Check your supply for lot number 1MP24069 with an expiration date of August 2026 (08/2026).
  3. Stop using the recalled product immediately. Healthcare facilities and clinics should quarantine the affected lot and contact Eugia US LLC or their distributor to arrange for the return of the product.
  4. If you have health concerns or believe you have experienced side effects from this medication, contact your healthcare provider or pharmacist.
  5. Call the FDA Consumer Complaint hotline at 1-888-723-3332 (1-888-SAFEFDA) for additional questions.

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, USP (150mg per mL)
Variants: 150mg per mL, 1 mL Single-Dose Vial
Lot Numbers:
1MP24069 (Exp 08/2026)
NDC:
55150-329-01

Manufactured in India for Eugia US LLC.

Additional Information

Agency: Food and Drug Administration (FDA)
Event ID: 96018
Status: Active
Manufacturer: Eugia US LLC
Sold By: Hospitals; Clinics; Wholesale distributors
Manufactured In: India
Units Affected: 19872 vials
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 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.