Cochlear recalls Baha 5 Sound Processor tamper proof battery doors due to incorrect packaging. Affected units have specific part and lot numbers. Consumers should check their product details to determine if recalled.
Product was packaged with the Incorrect tamper proof battery door.
Cochlear is recalling Baha 5 Sound Processor tamper proof battery doors because they were packaged with the wrong model. This issue doesn: t pose a safety risk but means the product may not function correctly.
The tamper proof battery door was packaged incorrectly, meaning it may not fit properly with the sound processor. This could cause the battery door to not seal correctly, leading to potential battery leakage or improper function.
Users of Cochlear Baha 5 Sound Processors with the specific tamper proof battery doors (part number P1129017) are affected. People who have the listed lot numbers are most at risk of receiving non-functional components.
Check for part number P1129017, UDI number 09321502041096, and lot number COH1253733 on the battery door packaging. The recall applies to the specific model of Baha 5 Sound Processor tamper proof battery doors.
Look for part number P1129017, UDI number 09321502041096, and lot number COH1253733 on the battery door packaging.
No, the recall is for incorrect packaging that may cause the battery door to not function properly, but it does not pose a safety risk.
Check for part number P1129017, UDI number 09321502041096, and lot number COH1253733 on the battery door packaging.
The recall does not require immediate action, but you should check if your product has the listed part and lot numbers to ensure proper function.
We’ve drafted a message you can send Cochlear to request your refund or repair — edit it as you like.
Subject: Recall Z-0792-2020 — Cochlear Cochlear Hello, I own a Cochlear that is covered by recall Z-0792-2020 from Cochlear. 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.
