US Drug Recall Register
Class II · Moderate risk Terminated Initiated Jun 12, 2023 (3 years ago)

Endometrin (progesterone) Vaginal Insert 100mg, packaged in a carton of 21 vaginal…

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

Why it was recalled

cGMP deviations: potential for Microbial Contamination of Non-Sterile Products

What was recalled

Endometrin (progesterone) Vaginal Insert 100mg, packaged in a carton of 21 vaginal inserts with 21 disposable vaginal applicators, Manufactured for: Ferring Pharmaceuticals Inc., Parsippany, NJ NDC# 55566-6500-03

Recalling firm
Ferring Pharmaceuticals Inc
NDC code
55566-6500-03
Origin
NJ, United States
Initiated by
N/A
FDA recall number
D-0879-2023

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.

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