Device recall
Z-1755-2010: The Baylis LumbarCool Pain Management Kit consisting of: 1 LumbarCool Pain…
FDA device recall · Class II · Baylis Medical Corp *
Key facts
| Recall number (Z-number) | Z-1755-2010 |
|---|---|
| Recall event | 55693 |
| Product | The Baylis LumbarCool Pain Management Kit consisting of: 1 LumbarCool Pain Management Probe, 3 LumbarCool Pain Management introducers, and 1 Pain Management Tube Kit. Model/Catalogue Number: LUK-17-150-4 The LumbarCool Pain Management System, a cooled radiofrequency pain management system, in… |
| Product code | GXI |
| Recalling firm | Baylis Medical Corp * |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Oct 4, 2010 |
| 510(k) numbers | K053082, K062937 |
| FEI number | 3005241199 |
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