US Drug Recall Register
Class II · Moderate risk Ongoing Initiated Jul 26, 2024 (2 years ago)

Progesterone Injection, USP, 500 mg per 10 mL (50mg/mL), 10 mL Multiple-Dose Vial, Rx…

Class II — Moderate risk. May cause temporary or reversible harm; serious harm unlikely.

Why it was recalled

Presence of Particulate Matter: Complaint received of a glass particle in the vial.

What was recalled

Progesterone Injection, USP, 500 mg 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.

Recalling firm
Eugia US LLC
NDC code
55150-306-10
Origin
NJ, United States
Initiated by
Voluntary: Firm initiated
FDA recall number
D-0624-2024

What should you do? A recall doesn't always mean your specific bottle is affected - it often applies to certain lots only. Check the lot number on your package against the FDA notice, and talk to your pharmacist before stopping any medication.

Other Progesterone recalls

See all