US Drug Recall Register
Class III · Low risk Terminated Initiated Sep 19, 2013 (13 years ago)

ENDOMETRIN (progesterone) Vaginal Insert 100 mg USP, 21 inserts, Rx Only, Manufactured…

Class III — Low risk. Unlikely to cause harm, but violates FDA regulations.

Why it was recalled

Discoloration; due to prolonged heat exposure.

What was recalled

ENDOMETRIN (progesterone) Vaginal Insert 100 mg USP, 21 inserts, Rx Only, Manufactured for: Ferring Pharmaceuticals Inc. Parsippany, NJ 07054 ---- NDC 55566-6500-3

Recalling firm
Ferring Pharmaceuticals Inc
NDC code
55566-6500-3
Origin
NJ, United States
Initiated by
Voluntary: Firm initiated
FDA recall number
D-1426-2014

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