Recall Z-0168-2023— Rebiscan, Inc.
Class II · Ongoing
Class II FDA medical device recall by Rebiscan, Inc., initiated 2022-10-03. 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: 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.
- Recalling firm
- Rebiscan, Inc.
- Classification
- Class II
- Status
- Ongoing
- Initiated
- 2022-10-03
- Firm location
- Boston, MA, United States
Product description
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
Data sourced from openFDA. This site is unofficial and independent of the FDA.