Device recall
Z-0872-06: Zimmer Cannulated Screw System Cannulated Driver, 5.0 mm Hex, REF 1147-49-50…
FDA device recall · Class II · Pioneer Surgical Technology
Key facts
| Recall number (Z-number) | Z-0872-06 |
|---|---|
| Recall event | 34922 |
| Product | Zimmer Cannulated Screw System Cannulated Driver, 5.0 mm Hex, REF 1147-49-50; Catalog # 00-1147-049-50. Manufactured by Pioneer Surgical Technology, Marquette, MI; Distributed by Zimmer, Warsaw, IN. |
| Product code | HWC |
| Recalling firm | Pioneer Surgical Technology |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Dec 4, 2007 |
| 510(k) numbers | K003496 |
| FEI number | 1000115331 |
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