Rebiscan recalls Blinq Pediatric Vision Scanners with battery packs that may vent and catch fire if unable to charge due to low cell voltage.
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
Rebiscan is recalling Blinq Pediatric Vision Scanners that have battery packs which may vent and catch fire if they can't charge properly. This could happen if the battery cells drop below 2.5 volts, which might occur during normal use.
The battery pack may not accept charge when cell voltage drops below 2.5 volts. This can cause the battery to vent and potentially catch fire, especially if the device is left charging for extended periods.
Parents and caregivers who own Blinq Pediatric Vision Scanners with specific serial numbers listed in the recall. Children using the device are at risk if the battery fails.
Check the serial numbers on the device: B-00001-V to B-00113. The model number is BQ830 with UDI 008648160004.
Ensure the battery pack can charge by testing if it accepts power when cell voltage is above 2.5 volts.
Reach out to Rebiscan for specific guidance on battery safety and potential remedies.
The battery pack may vent and catch fire if it cannot charge properly due to low cell voltage, which could happen during normal use.
Check the serial numbers: B-00001-V to B-00113. The model number is BQ830 with UDI 008648160004.
Contact Rebiscan for specific guidance on battery safety and potential remedies.
We’ve drafted a message you can send Rebiscan to request your refund or repair — edit it as you like.
Subject: Recall Z-0168-2023 — Rebiscan Rebiscan Hello, I own a Rebiscan that is covered by recall Z-0168-2023 from Rebiscan. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.