Device recall
Z-0721-2010: Stryker CBC Blood Conservation Kit with Quick Disconnect Blood Bag, sterile…
FDA device recall · Class II · Stryker Instruments Div. of Stryker Corporation
Key facts
| Recall number (Z-number) | Z-0721-2010 |
|---|---|
| Recall event | 54149 |
| Product | Stryker CBC Blood Conservation Kit with Quick Disconnect Blood Bag, sterile, Stryker Instruments, Kalamazoo, MI, REF 225-28-85. Blood recovery system used post-operatively to collect, filter and allow for reinfusion of autologous blood. |
| Product code | cac |
| Recalling firm | Stryker Instruments Div. of Stryker Corporation |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Oct 25, 2010 |
| 510(k) numbers | K952224 |
| FEI number | 1811755 |
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