Device recall
Z-1235-03: CaverMap Surgical Aid Disposable Kit with Focused Probe Tip, Sterile Part…
FDA device recall · Class II · Blue Torch Medical Technologies
Key facts
| Recall number (Z-number) | Z-1235-03 |
|---|---|
| Recall event | 27068 |
| Product | CaverMap Surgical Aid Disposable Kit with Focused Probe Tip, Sterile Part Number: 8305 |
| Recalling firm | Blue Torch Medical Technologies |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Oct 22, 2003 |
| 510(k) numbers | K000507, K993436 |
| FEI number | 3004115203 |
At a glance
- 1–9 Linked 510(k)s
- 1–9 Products in the same recall event
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