Device recall
Z-0228-04: Model LightLas 532 Opthalmic Photocoagulator Laser
FDA device recall · Class II · LightMed USA Inc
Key facts
| Recall number (Z-number) | Z-0228-04 |
|---|---|
| Recall event | 27819 |
| Product | Model LightLas 532 Opthalmic Photocoagulator Laser |
| Product code | HQF |
| Recalling firm | LightMed USA Inc |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Dec 16, 2003 |
| 510(k) numbers | K010372 |
| FEI number | 3003976404 |
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