Device recall
Z-2512-2023: PHOROPTOR VRX DIGITAL REFRACTION SYSTEM-Digital refractor intended for the…
FDA device recall · Class II · Reichert, Inc.
Key facts
| Recall number (Z-number) | Z-2512-2023 |
|---|---|
| Recall event | 92805 |
| Product | PHOROPTOR VRX DIGITAL REFRACTION SYSTEM-Digital refractor intended for the subjective measurement of the refractive error of the eye. MODEL NUMBER: 16242 [Model 16241 is the base model. Model 16242 includes an additional prism feature used for the measurement of ocular deviation in patients with… |
| Product code | HKN |
| Recalling firm | Reichert, Inc. |
| Recall class | Class II |
| Status | Open, Classified |
| FEI number | 1000159913 |
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