Drug recall
ENDOMETRIN (progesterone) Vaginal Insert 100 mg USP, 21 inserts, Rx Only, Manufactured for: Ferring…
FDA recall event 66604 · Class III · Ferring Pharmaceuticals Inc
Key facts
| Event ID | 66604 |
|---|---|
| Recall numbers | D-1426-2014 |
| Recalling firm | Ferring Pharmaceuticals Inc |
| Product type | Drugs |
| Products | ENDOMETRIN (progesterone) Vaginal Insert 100 mg USP, 21 inserts, Rx Only, Manufactured for: Ferring Pharmaceuticals Inc. Parsippany, NJ 07054 ---- NDC 55566-6500-3 |
| Classification | Class III |
| Status | Terminated |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | Discoloration; due to prolonged heat exposure. |
| Initiation date | Sep 19, 2013 |
| Report date | Jul 16, 2014 |
| Termination date | Feb 19, 2015 |
| City | Parsippany |
| State | NJ |
| Country | United States |
| FEI number | 1000119907 |
At a glance
- 1–9 Products in this recall
- None FDA inspections of this firm (FEI)
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About FDA drug and product recalls
FDA enforcement reports list recalls of drugs, biologics, foods and other FDA-regulated products, classified by the potential health hazard.
Source: U.S. Food and Drug Administration (FDA), Enforcement Reports · Source date: