Device recall
Z-0171-04: Stryker brand OrthoTec pulsed irrigation/suction handpiece and tubing set; part…
FDA device recall · Class II · Stryker Instruments, Instruments Div.
Key facts
| Recall number (Z-number) | Z-0171-04 |
|---|---|
| Recall event | 27690 |
| Product | Stryker brand OrthoTec pulsed irrigation/suction handpiece and tubing set; part number 0203-020-000. |
| Product code | FPK |
| Recalling firm | Stryker Instruments, Instruments Div. |
| Recall class | Class II |
| Status | Terminated |
| Termination date | May 3, 2004 |
| FEI number | 1811755 |
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