Product Wiki · Recalls · U.S. FDA — Device Enforcement

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 Processor (CI-5280), Na¿da CI Q70 Sound Processor (CI-5245) and Na¿da CI Q30 Sound Processor (CI-5260) for cochlear implant.

U.S. FDA — Device Enforcement · United States · 2020-09-26 · Class III

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-0486-2021
Date of alert
2020-09-26
Country / jurisdiction
United States
Risk level
Class III
Risk type
recall
Brand
Advanced Bionics, LLC
Product category
device
Product type
Devices
Barcode (EAN/GTIN)
410079020
Reported risk: Mislabeling; It has been determined that some batteries were improperly labeled and may contain a different battery life than indicated.
Primary source: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts

Verify each fact at the issuing agency before acting. Recall scope, affected lots, and remediation instructions may be updated by the agency after our last sync.

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ProductGuru indexes recall and safety-alert records from ~30 public agency registries. We are not lawyers, regulators or product-safety consultants. This page restates what the named agency published; consult the primary source above (or qualified counsel in your jurisdiction) before any commercial, medical or safety decision.