Device recall
Z-2950-2011: CAPIOX Flexible Venous Reservoirs, 1500 mL, product codes: CXFVR1500X and…
FDA device recall · Class II · Terumo Cardiovascular Corporation
Key facts
| Recall number (Z-number) | Z-2950-2011 |
|---|---|
| Recall event | 59454 |
| Product | CAPIOX Flexible Venous Reservoirs, 1500 mL, product codes: CXFVR1500X and CXFVRI500XC, used singly or packaged as components in cardiovascular procedure trays labeled in part ***Terumo Caerdiovascular Systems Corporation, Elkton, MD 21921*** Product Usage: The reservoir bag is intended for use as a… |
| Product code | DTN |
| Recalling firm | Terumo Cardiovascular Corporation |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Feb 10, 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