Device recall
Z-1066-04: Surgical powered laser instrument, used for photocoagulation of ocular tissues…
FDA device recall · Class I · Carl Zeiss Ophthalmic Systems Inc
Key facts
| Recall number (Z-number) | Z-1066-04 |
|---|---|
| Recall event | 29367 |
| Product | Surgical powered laser instrument, used for photocoagulation of ocular tissues in the treatment of diseases of the eye. |
| Product code | GEX |
| Recalling firm | Carl Zeiss Ophthalmic Systems Inc |
| Recall class | Class I |
| Status | Terminated |
| Termination date | Jan 11, 2005 |
| 510(k) numbers | K013402 |
| FEI number | 2918630 |
At a glance
- 1–9 Linked 510(k)s
- 1–9 Products in the same recall event
- 100–999 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