Device recall
Z-1709-2014: CARINAsim MAN-1236 Rev 2 and CARINAiso MAN-1237 Rev 2 laser software. LAP…
FDA device recall · Class II · LAP of America Laser Applications, LLC
Key facts
| Recall number (Z-number) | Z-1709-2014 |
|---|---|
| Recall event | 68266 |
| Product | CARINAsim MAN-1236 Rev 2 and CARINAiso MAN-1237 Rev 2 laser software. LAP isocenter marking control software. Laser systems for patient alignment. |
| Recalling firm | LAP of America Laser Applications, LLC |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Sep 14, 2016 |
| FEI number | 1000113153 |
At a glance
- None 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