Device recall
Z-0168-2023: Blinq Pediatric Vision Scanner-Pediatric Vision Scanner-intended for automated…
FDA device recall · Class II · Rebiscan, Inc.
Key facts
| Recall number (Z-number) | Z-0168-2023 |
|---|---|
| Recall event | 90968 |
| Product | Blinq Pediatric Vision Scanner-Pediatric Vision Scanner-intended for automated detection of misalignment of the visual axes using polarized light. Model Number BQ830 |
| Product code | PMW |
| Recalling firm | Rebiscan, Inc. |
| Recall class | Class II |
| Status | Open, Classified |
| FEI number | 3014522421 |
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