AB PowerCel 170 — Class III medical device recall Z-0487-2021
Terminated recall by Advanced Bionics, LLC, reported 2020-12-02, distributed nationwide. Mislabeling; It has been determined that some batteries were improperly labeled and may contain a different ba
| Recall number | Z-0487-2021 |
|---|---|
| Product type | Medical device |
| Classification | Class III |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Advanced Bionics, LLC, Valencia, CA, United States |
| Recall initiated | 2020-09-26 |
| Classified | 2020-11-25 |
| Reported by FDA | 2020-12-02 |
| Terminated | 2023-05-04 |
| Distributed | Nationwide (US) |
| Countries outside the US | BE, CO, CZ, DE, ES, IR, IT, KW, NL, PA, PE, TW |
| Quantity | 28 units |
| Reason classes | labeling |
| UPC / GTIN / UDI-DI | 07630016833113 |
| Model numbers | CI-5517-150 |
Product
AB PowerCel 170 (velvet black), REF: CI-5517-150, UDI: (01) 07630016833113 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 for recall
Mislabeling; It has been determined that some batteries were improperly labeled and may contain a different battery life than indicated.
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-0487-2021. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.