Device recall
Z-1303-2013: Curity I.V. Start Kit, Product ID: 80530 and Curity I.V. Start Kit Product ID…
FDA device recall · Class III · Covidien LLC
Key facts
| Recall number (Z-number) | Z-1303-2013 |
|---|---|
| Recall event | 64908 |
| Product | Curity I.V. Start Kit, Product ID: 80530 and Curity I.V. Start Kit Product ID: 8508. IV Start Kit. |
| Product code | LRS |
| Recalling firm | Covidien LLC |
| Recall class | Class III |
| Status | Terminated |
| Termination date | Jun 2, 2015 |
| 510(k) numbers | K842898 |
| FEI number | 1282497 |
At a glance
- 1–9 Linked 510(k)s
- 1–9 Products in the same recall event
- 100–999 Recalled products with this product code
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About FDA device recalls (products)
Each recalled device product receives a Z-number. Recall details such as root cause, distribution and firm actions are available in Orca1.
Source: U.S. Food and Drug Administration (FDA), Medical Device Recalls database