Device recall
Z-0614-2021: Carl Zeiss Meditec AG VISUREF150 REF 2227-967 - Product Usage: is a diagnostic…
FDA device recall · Class II · Carl Zeiss Meditec AG
Key facts
| Recall number (Z-number) | Z-0614-2021 |
|---|---|
| Recall event | 86366 |
| Product | Carl Zeiss Meditec AG VISUREF150 REF 2227-967 - Product Usage: is a diagnostic instrument used to determine the objective refractive values and keratometric characteristics of the human eye. The results are used to assist the process of prescribing optical aids such as eyeglasses and contact lenses. |
| Product code | HKO |
| Recalling firm | Carl Zeiss Meditec AG |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Dec 13, 2024 |
| FEI number | 3001362763 |
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