Device recall
Z-0165-06: Biosteon brand HA/PLLA Cross Pin, Model Number 234-500-350; Product is…
FDA device recall · Class III · Stryker Endoscopy
Key facts
| Recall number (Z-number) | Z-0165-06 |
|---|---|
| Recall event | 33186 |
| Product | Biosteon brand HA/PLLA Cross Pin, Model Number 234-500-350; Product is distributed by Stryker Endoscopy, 5900 Optical Court, San Jose, CA 95138 |
| Product code | HWC |
| Recalling firm | Stryker Endoscopy |
| Recall class | Class III |
| Status | Terminated |
| Termination date | Nov 21, 2005 |
| 510(k) numbers | K021351 |
| 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