# FDA recall Z-0168-2023

> **Rebiscan, Inc.** · Class II · device recall 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 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

## Distribution

Worldwide distribution - US Nationwide and the countries of New Zealand, Belgium.

## Key facts

- **Recall number:** Z-0168-2023
- **Recalling firm:** Rebiscan, Inc.
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2022-10-03
- **Report date:** 2022-11-09

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Boston, MA, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-0168-2023

## Citation

> AI Analytics. FDA recall Z-0168-2023. Retrieved 2026-06-09 from https://api.ai-analytics.org/recall/Z-0168-2023. Source: US FDA. Licensed CC0.

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