Device recall
Z-2573-2014: STREAMLINE CT CERVICO-THORACIC SYSTEM; SET SCREW REF 26-SETSCREW NON-STERILE…
FDA device recall · Class II · PIONEER SURGICAL TECHNOLOGY, INC.
Key facts
| Recall number (Z-number) | Z-2573-2014 |
|---|---|
| Recall event | 69033 |
| Product | STREAMLINE CT CERVICO-THORACIC SYSTEM; SET SCREW REF 26-SETSCREW NON-STERILE, SINGLE USE, RX ONLY |
| Product code | KWP |
| Recalling firm | PIONEER SURGICAL TECHNOLOGY, INC. |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Sep 30, 2014 |
| 510(k) numbers | K112757 |
| FEI number | 1000115331 |
At a glance
- 1–9 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