Device recall
Z-2399-2010: Peregrine 20 GA Endo Ocular Adjustable Laser Probe
FDA device recall · Class II · Peregrine Surgical Ltd
Key facts
| Recall number (Z-number) | Z-2399-2010 |
|---|---|
| Recall event | 56271 |
| Product | Peregrine 20 GA Endo Ocular Adjustable Laser Probe |
| Product code | HQF |
| Recalling firm | Peregrine Surgical Ltd |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Sep 30, 2010 |
| FEI number | 1000121498 |
At a glance
- None 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