RecallRadar

FDA Drug recall D-1426-2014

ENDOMETRIN (progesterone) Vaginal Insert 100 mg USP, 21 inserts, Rx Only, Manufactured for: Ferring Pharmaceuticals Inc

On 2014-07-16 the FDA classified a Class III recall of ENDOMETRIN (progesterone) Vaginal Insert 100 mg USP, 21 inserts, Rx Only, Manufactured for: Ferring Pharmaceuticals Inc by Ferring Pharmaceuticals, citing discoloration; due to prolonged heat exposure.

Read the official FDA Drug notice

AgencyFDA Drug
Recall numberD-1426-2014
ClassificationClass III
Statusterminated
Initiated2013-09-19
Published2014-07-16
Last updated2026-09-13 11:51 UTC
CompanyFerring Pharmaceuticals
DistributionUS

Product

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

Reason

Discoloration; due to prolonged heat exposure.

Identifiers

ndc55566-6500-1
ndc55566-6500-2
ndc55566-6500-3
ndc55566-6500-4
ndc55566-6500-7
ndc55566-6500-8
code_info
Lot Number:Expiry Date - 0804.182B-1:07/14; 0804.183B-1:07/14; 0804.185A-1:08/14; 0804.186B-1:08/14; 0804.187B-1:08/14;…Lot Number:Expiry Date - 0804.182B-1:07/14; 0804.183B-1:07/14; 0804.185A-1:08/14; 0804.186B-1:08/14; 0804.187B-1:08/14; 0804.210A-1:12/14; 0804.212A-1:12/14; 0804.213A-1:12/14; 0804.214A-1:12/14; 0804.216B-1:12/14; 0804.223B-1:02/15 0804.225B-1:03/15

Status history

No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:51 UTC. Current status: terminated.

Source

Official record: https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-1426-2014%22

RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.