Device recall
Z-0236-2007: Terumo Perfusion System 8000 Base, 4 pump, 115v; Model 8000; Catalog No. 16400.
FDA device recall · Class II · Terumo Cardiovascular Systems Corp
Key facts
| Recall number (Z-number) | Z-0236-2007 |
|---|---|
| Recall event | 36150 |
| Product | Terumo Perfusion System 8000 Base, 4 pump, 115v; Model 8000; Catalog No. 16400. |
| Product code | DTW |
| Recalling firm | Terumo Cardiovascular Systems Corp |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Jun 19, 2008 |
| 510(k) numbers | K915183 |
| FEI number | 1828100 |
At a glance
- 1–9 Linked 510(k)s
- 10–99 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