Device recall
Z-0410-2009: PALINDROME EMERALD Kit - Cuffed Dual Lumen Catheter with Pre-curved Shaft and…
FDA device recall · Class III · Covidien
Key facts
| Recall number (Z-number) | Z-0410-2009 |
|---|---|
| Recall event | 50081 |
| Product | PALINDROME EMERALD Kit - Cuffed Dual Lumen Catheter with Pre-curved Shaft and Heparin Coating, REF 8888145069, 14.5 Fr/CH (4.85mm) x 23cm. TYCO HEALTHCARE GROUP LP, Mansfield, MA 02048. --- NOTE: Both the "sport pack" and "kit" package configurations include the catheter, Venetrac insertion stylets… |
| Product code | NYU |
| Recalling firm | Covidien |
| Recall class | Class III |
| Status | Terminated |
| Termination date | Dec 4, 2008 |
| 510(k) numbers | K051584 |
| FEI number | 1317749 |
At a glance
- 1–9 Linked 510(k)s
- 1–9 Products in the same recall event
- 10–99 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