Eugia US LLC recalls 500 mg progesterone injections due to glass particles in vials. Affected lots from India manufacturing; stop using if you have this product.
Presence of Particulate Matter: Complaint received of a glass particle in the vial.
Eugia US LLC is recalling progesterone injections that may contain glass particles. This could cause injury if injected. The recall affects specific lots manufactured in India.
Glass particles in the vial could cause injury if injected. This is a known issue with some medical injections that may lead to tissue damage or other complications.
People who have the recalled progesterone injection vials (NDC 55150-306-10) from India manufacturing. Healthcare providers using this product for medical treatment are most at risk.
Check for the product name 'Progesterone Injection, USP, 500 mg per 10 mL (50mg/mL), 10 mL Multiple-Dose Vial'. Look for the lot number CPR230029A on the vial.
Verify the product name and lot number CPR230029A on the vial.
The recall states there is a complaint of glass particles, but the product is not safe to use without checking the lot number.
The recall does not specify a remedy, so contact Eugia US LLC for guidance.
Check for the product name and lot number CPR230029A on the vial.
We’ve drafted a message you can send Eugia to request your refund or repair — edit it as you like.
Subject: Recall D-0624-2024 — Eugia Eugia Hello, I own a Eugia that is covered by recall D-0624-2024 from Eugia. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
