Device recall
Z-1351-2022: Philips Laser System, REF LAS-100, Intermittent Operation, Duty cycle dependent…
FDA device recall · Class II · Spectranetics Corporation
Key facts
| Recall number (Z-number) | Z-1351-2022 |
|---|---|
| Recall event | 90364 |
| Product | Philips Laser System, REF LAS-100, Intermittent Operation, Duty cycle dependent upon device in use 100 - 240 VAC, 50/60HZ, 16 AM |
| Product code | LPC |
| Recalling firm | Spectranetics Corporation |
| Recall class | Class II |
| Status | Open, Classified |
| PMA numbers | P910001, P910001S115 |
| FEI number | 3007284006 |
At a glance
- None Linked 510(k)s
- 1–9 Products in the same recall event
- 1–9 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