Boston, MA, United States
Rebiscan, Inc. recalls
1 recall recorded since 2018, most recently on 3 October 2022. 1 is listed as ongoing. Status and classification are as published by the FDA.
Recalls1
Ongoing (FDA)1
Terminated or completed0
Class I (FDA)0
Ongoing Class II Medical devices
- Recall started
- 3 October 2022
- 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
- Distribution
- Worldwide distribution - US Nationwide and the countries of New Zealand, Belgium.
- Initiated
- Voluntary: Firm initiated
- Recall number
- Z-0168-2023
- Blinq Pediatric Vision Scanner-Pediatric Vision Scanner-intended for automated detection of misalignment of the visual axes using polarized light. Model Number BQ830
A terminated FDA recall means the FDA has determined that all reasonable efforts to remove or correct the product have been made. What statuses mean.