Device recall
Z-2193-2010: Crossfire Console, model number 475-000-000, Manufactured by Stryker Endoscopy…
FDA device recall · Class II · Stryker Endoscopy
Key facts
| Recall number (Z-number) | Z-2193-2010 |
|---|---|
| Recall event | 56321 |
| Product | Crossfire Console, model number 475-000-000, Manufactured by Stryker Endoscopy San Jose Medical device indicated for use in orthopedic and arthroscopic procedures for the knee, shoulder, ankle, elbow, wrist and hip. The system provides abrasion, resection, debridement, and removal of bone and soft… |
| Product code | GEI |
| Recalling firm | Stryker Endoscopy |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Mar 21, 2011 |
| 510(k) numbers | K071859 |
| FEI number | 2936485 |
At a glance
- 1–9 Linked 510(k)s
- 1–9 Products in the same recall event
- 100–999 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