Drug recall
Curity I.V. Start Kit, Product ID: 80530 and Curity I.V. Start Kit Product ID: 8508. IV Start Kit.
FDA recall event 64908 · Class III · Covidien LLC
Key facts
| Event ID | 64908 |
|---|---|
| Recall numbers | Z-1303-2013, Z-1304-2013 |
| Recalling firm | Covidien LLC |
| Product type | Devices |
| Products | Curity I.V. Start Kit, Product ID: 80530 and Curity I.V. Start Kit Product ID: 8508. IV Start Kit., Curity Staple Remover Kit; Product Code: 66701. Staple Remover Kit. |
| Classification | Class III |
| Status | Terminated |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | On March 26, 2013 Covidien received a recall notice from one of their suppliers CareFusion. CareFusion is recalling a variety of OTC drug products including the 10% Povidone Iodine SEPP Applicator… |
| Initiation date | Apr 12, 2013 |
| Report date | May 22, 2013 |
| Termination date | Jun 2, 2015 |
| City | Mansfield |
| State | MA |
| Country | United States |
| FEI number | 1282497 |
At a glance
- 1–9 Products in this recall
- 10–99 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: