FDA Device recall Z-0486-2021
AB PowerCel 230 (velvet black), REF: CI-5523-150, UDI: (01) 07630016832956 used to power the following devices: Na¿da CI Q90 Sound Processo…
- FDA Device
- Class III
- terminated
- Published 2020-12-02
On 2020-12-02 the FDA classified a Class III recall of AB PowerCel 230 (velvet black), REF: CI-5523-150, UDI: (01) 07630016832956 used to power the following devices: Na¿da CI Q90 Sound Processo… by Advanced Bionics, citing mislabeling; It has been determined that some batteries were improperly labeled and may contain a different battery life than indicated.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-0486-2021 |
| Classification | Class III |
| Status | terminated |
| Initiated | 2020-09-26 |
| Published | 2020-12-02 |
| Last updated | 2026-09-13 11:55 UTC |
| Company | Advanced Bionics |
| Distribution | US |
Product
AB PowerCel 230 (velvet black), REF: CI-5523-150, UDI: (01) 07630016832956 used to power the following devices: Na¿da CI Q90 Sound Processor (CI-5280), Na¿da CI Q70 Sound Processor (CI-5245) and Na¿da CI Q30 Sound Processor (CI-5260) for cochlear implant.
Reason
Mislabeling; It has been determined that some batteries were improperly labeled and may contain a different battery life than indicated.
Identifiers
| code_info | 410079020 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:55 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0486-2021%22
RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.