Device recall
Z-2606-2010: Sarns Centrifugal Pump with X-Coating, packaged within custom ordered…
FDA device recall · Class II · Terumo Cardiovascular Corporation
Key facts
| Recall number (Z-number) | Z-2606-2010 |
|---|---|
| Recall event | 56322 |
| Product | Sarns Centrifugal Pump with X-Coating, packaged within custom ordered Cardiovascular Procedure Kits, P/N 3ZZ164275X, 3ZZ164275, CEOT028, CEOT032; and as single sterile units with product codes CV-164275, 164275 and 164275X. CV-164275 is an item number for product that is sold to foreign affiliate… |
| Product code | KFM |
| Recalling firm | Terumo Cardiovascular Corporation |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Nov 4, 2011 |
| 510(k) numbers | K020998 |
| FEI number | 3000204839 |
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