Device recall
Z-2614-2010: Cardiovascular Procedure Kit X-Coated Pump and Table Pack, Item #71552
FDA device recall · Class II · Terumo Cardiovascular Corporation
Key facts
| Recall number (Z-number) | Z-2614-2010 |
|---|---|
| Recall event | 56413 |
| Product | Cardiovascular Procedure Kit X-Coated Pump and Table Pack, Item #71552 |
| Product code | DTR |
| Recalling firm | Terumo Cardiovascular Corporation |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Feb 29, 2012 |
| FEI number | 3000204839 |
At a glance
- None 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