ENDOMETRIN — Class III drug recall D-1426-2014
Terminated recall by Ferring Pharmaceuticals Inc, reported 2014-07-16, distributed nationwide. Discoloration; due to prolonged heat exposure.
| Recall number | D-1426-2014 |
|---|---|
| Product type | Drug |
| Classification | Class III |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Ferring Pharmaceuticals Inc, Parsippany, NJ, United States |
| Recall initiated | 2013-09-19 |
| Classified | 2014-07-09 |
| Reported by FDA | 2014-07-16 |
| Terminated | 2015-02-19 |
| Distributed | Nationwide (US) |
| Quantity | 72,046 cartons |
| NDC | 55566-6500, 55566-6500-01, 55566-6500-02, 55566-6500-03, 55566-6500-04, 55566-6500-07, 55566-6500-08 |
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 for recall
Discoloration; due to prolonged heat exposure.
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/D-1426-2014. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.