Blinq Pediatric Vision Scanner-Pediatric Vision Scanner-intended for… — Class II medical device recall Z-0168-2023
Ongoing recall by Rebiscan, Inc., reported 2022-11-09, distributed nationwide. Unable to charge the battery pack- battery packs will allow the batteries to be charged if the voltage of any
| Recall number | Z-0168-2023 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Ongoing |
| Voluntary or mandated | Voluntary |
| Recalling firm | Rebiscan, Inc., Boston, MA, United States |
| Recall initiated | 2022-10-03 |
| Classified | 2022-11-01 |
| Reported by FDA | 2022-11-09 |
| Distributed | Nationwide (US) |
| Countries outside the US | BE, NZ |
| Quantity | 63 units |
| Serial numbers | B-00001-V |
| Model numbers | BQ830 |
Product
Blinq Pediatric Vision Scanner-Pediatric Vision Scanner-intended for automated detection of misalignment of the visual axes using polarized light. Model Number BQ830
Reason for recall
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
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-0168-2023. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.