Advanced Bionics recalls some AB PowerCel 170 (velvet black) batteries for potential mislabeling that could lead to incorrect battery life claims. Affected units were sold with specific cochlear implant devices.
Mislabeling; It has been determined that some batteries were improperly labeled and may contain a different battery life than indicated.
Advanced Bionics is recalling some AB PowerCel 170 (velvet black) batteries that may have incorrect battery life labels. This could cause users to think their batteries last longer than they actually do, potentially affecting device performance.
The batteries may have been mislabeled, meaning the actual battery life could differ from what's advertised. This might lead to unexpected device shutdowns or reduced functionality for cochlear implant users.
Users of specific cochlear implant devices (Na¿da CI Q30, Q70, Q90 Sound Processors) who own the recalled battery model. People with cochlear implants are most at risk.
Check for the battery model 'AB PowerCel 170 (velvet black)' with reference number CI-5517-150 and unique identifier (01) 07630016833113. These batteries power specific Na¿da cochlear implant devices.
Look for the reference number CI-5517-150 and unique identifier (01) 07630016833113 on the battery.
The recalled batteries power Na¿da CI Q30, CI Q70, and CI Q90 Sound Processors.
Some batteries were improperly labeled and may have a different battery life than indicated.
No action is required beyond checking the label; the recall is for potential mislabeling, not immediate safety risks.
We’ve drafted a message you can send Advanced Bionics to request your refund or repair — edit it as you like.
Subject: Recall Z-0487-2021 — Advanced Bionics Advanced Bionics Hello, I own a Advanced Bionics that is covered by recall Z-0487-2021 from Advanced Bionics. 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.
