Key Takeaway

ENDOMETRIN (progesterone) Vaginal Insert 100 mg USP, 21 inserts, Rx Only, Manufactured for: Ferring Pharmaceuticals Inc. Parsippany, NJ 07054 ---- NDC 55566-6500-3 by Ferring Pharmaceuticals Inc was recalled on September 19, 2013. The hazard: Discoloration; due to prolonged heat exposure.

FDA Drug Class III Terminated

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

Recalled: September 19, 2013 ~72,046 cartons units affected D-1426-2014

Description

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

Hazard / Reason

Discoloration; due to prolonged heat exposure.

Class III: Product that is not likely to cause adverse health consequences.

Class III is the least severe classification. The product is unlikely to cause adverse health consequences but still violates FDA regulations.

Products Affected

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

Drugs

Company Information

Ferring Pharmaceuticals Inc

Parsippany, NJ, United States

View all 12 recalls by Ferring Pharmaceuticals Inc →

Distribution

Nationwide.

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Frequently Asked Questions

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