Device recall
Z-1007-2022: ZEISS miLOOP Lens Fragmentation Device REF 303071-9090-000. Used during cataract…
FDA device recall · Class II · Carl Zeiss Meditec AG
Key facts
| Recall number (Z-number) | Z-1007-2022 |
|---|---|
| Recall event | 89928 |
| Product | ZEISS miLOOP Lens Fragmentation Device REF 303071-9090-000. Used during cataract surgery. |
| Product code | HNQ |
| Recalling firm | Carl Zeiss Meditec AG |
| Recall class | Class II |
| Status | Open, Classified |
| FEI number | 3003481798 |
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