Drug recall
ParaGard T 380A - Intrauterine Copper Contraceptive, 176 mg of copper wire, Duramed Pharmaceuticals Inc, a…
FDA recall event 67809 · Class II · Teva Pharmaceuticals USA
Key facts
| Event ID | 67809 |
|---|---|
| Recall numbers | D-1354-2014 |
| Recalling firm | Teva Pharmaceuticals USA |
| Product type | Drugs |
| Products | ParaGard T 380A - Intrauterine Copper Contraceptive, 176 mg of copper wire, Duramed Pharmaceuticals Inc, a subsidiary of Barr Pharmaceuticals, Inc., Pomona, NY |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | Non-sterility: due to a failed sterility test |
| Initiation date | Mar 21, 2014 |
| Report date | Jun 4, 2014 |
| Termination date | Nov 14, 2014 |
| City | Horsham |
| State | PA |
| Country | United States |
| FEI number | 3003092769 |
At a glance
- 1–9 Products in this recall
- 1–9 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: