FDA recall record

Progesterone Injection USP, 500mg per 10 mL (50mg/mL), 10 mL Multiple Dose Vial recall — FDA D-0186-2025

Presence of Particulate Matter: A market complaint was received of a glass piece in the vial.

Class IIclassification
D-0186-2025official record ID
Jan 15, 2025report date

Recall record at a glance

Official recordD-0186-2025
CategoryDrug Recalls
ClassificationClass II
FDA record statusOngoing
Recalling firmEugia US LLC
Report dateJan 15, 2025
Recall initiation dateDec 27, 2024
Quantity17,300 10-mL vials
LocationEast Windsor, NJ, United States

Official product description

Progesterone Injection USP, 500mg per 10 mL (50mg/mL), 10 mL Multiple Dose Vial, Rx Only, Mfd. in India for: Eugia US LLC. E. Windsor NJ 08520 NDC # 55150-306-10

Why the product was recalled

Presence of Particulate Matter: A market complaint was received of a glass piece in the vial.

Distribution information

Distributed Nationwide in the USA.

How to read the classification

FDA Class II indicates a situation in which use of or exposure to the product may cause temporary or medically reversible adverse health consequences, or where the probability of serious consequences is remote. The classification shown here comes from the FDA record.

Additional record details

Recall type: Voluntary: Firm initiated. Initial notification: Letter.

What to do next

If you believe you have the recalled product, use the recall number and firm information above to confirm the official notice and follow the instructions issued by the FDA, recalling firm, retailer or product manufacturer. For drugs and medical devices, decisions about treatment or medical care should be discussed with a qualified health professional.

About this record

Recall Lookup USA preserves the most complete source information successfully retrieved. We do not create missing facts or infer affected lots or VINs. The official record may still change, so use the identifier above when verifying current instructions.

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