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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

Eugia Progesterone Injection USP Recalled for Glass Particulate Matter

Agency Publication Date: January 7, 2025
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Summary

Eugia US LLC has voluntarily recalled 17,300 vials of Progesterone Injection USP, 500mg per 10 mL (50mg/mL). The recall was issued after a consumer report indicated that a piece of glass was found inside a 10 mL multiple-dose vial. This prescription medication is used for hormone replacement and was distributed nationwide to wholesalers and healthcare providers.

Risk

Injecting a product containing glass particles can cause local irritation, inflammation, or damage to blood vessels and organs. If the glass fragment enters the bloodstream, it could lead to serious medical complications, including blockages or damage to internal tissues.

What You Should Do

  1. This recall affects Progesterone Injection USP, 500mg per 10 mL (50mg/mL) sold in 10 mL multiple-dose vials under NDC 55150-306-10.
  2. The specific units affected are from Batch # 1PR24010 with an expiration date of 02/28/2027.
  3. If you have health concerns, contact your healthcare provider or pharmacist. Return any unused product to the place of purchase for a refund, throw it away, or contact the manufacturer for further instructions.
  4. Call the FDA Consumer Complaint hotline at 1-888-723-3332 (1-888-SAFEFDA) or visit www.fda.gov/safety/recalls for more information.

Your Remedy Options

You have 2 options:

๐Ÿ’ฐOption 1: Full Refund
How to: Contact your healthcare provider or pharmacist for guidance, or return any unused product to the place of purchase for a refund
๐Ÿ—‘๏ธOption 2: Dispose of Product
How to: Throw the product away. For prescription medications, a DEA take-back location or pharmacy mail-back program is preferred when available.

Affected Products

Product: Progesterone Injection USP, 500mg per 10 mL (50mg/mL)by Eugia US LLC
Variants: 10 mL Multiple Dose Vial, Rx Only
Lot Numbers:
1PR24010 (Exp 02/28/2027)
NDC:
55150-306-10

Manufactured in India for Eugia US LLC.

Additional Information

Agency: Food and Drug Administration (FDA)
Event ID: 96073
Status: Active
Manufacturer: Eugia US LLC
Sold By: Wholesalers; Healthcare providers
Manufactured In: India
Units Affected: 17,300 10-mL 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.