Class II — Rebiscan, Inc.
| Recalling firm | Rebiscan, Inc. |
|---|---|
| Registered facility | REBISCAN, INC. (the firm's only registered facility) |
| Classification | Class II |
| Status | Ongoing |
| Reason | Unable to charge the battery pack- battery packs will allow the batteries to be charged if the voltage of any cell is below 2.5V. When this occurs, the battery pack will not accept the charge, could vent and possibly catch fire |
| Product | Blinq Pediatric Vision Scanner-Pediatric Vision Scanner-intended for automated detection of misalignment of the visual axes using polarized light. Model Number BQ830 |
| Quantity | 63 units |
| Distribution | Worldwide distribution - US Nationwide and the countries of New Zealand, Belgium. |
| Initiated | 2022-10-03 |
| Classified | 2022-11-01 |
| Recall number | Z-0168-2023 |
| Initiation | Voluntary: Firm initiated |
Source: U.S. FDA via openFDA (opens in a new tab) (device registration & enforcement). Data as of 2026-10-06. Verify this recall record at FDA → (opens in a new tab)
Cite this record
RegWarden. “Class II recall — Rebiscan, Inc. (Z-0168-2023).” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/recall/90968/
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