Naida CI Q30Recalls & reported problems across all models

We found 3 models of Naida CI Q30 by Advanced Bionics, LLC in the FDA's device registry (GUDID). None of them is named in an adverse event report in our data.

1 FDA recall record name at least one of these models by its device identifier.

Reports come from manufacturers, hospitals and patients and are not verified by the FDA. A report does not prove the device caused the event. Widely used products collect more reports, so totals can't be used to compare products or estimate failure rates. Only reports that name a model's exact device identifier are counted. What reports can and can't tell you · How this data works

Naida CI Q30 recalls

FDA recall records that name at least one of these models by its device identifier, newest first. Each recall usually covers specific models or lots, so check the details.

1. Feb 6, 2019Terminated

   The sound processors were loaded with the incorrect firmware.

   Z-1083-2019 · Root cause: Process control · names 3 of these models · Recall details · FDA record ↗

Naida CI Q30 models

3 models, most reported first. Each model has its own page with its reports, recalls and device details.

• Naida CI Q30 CI-5260-140

  IMPLANT, COCHLEAR
  1 recall0 reports
• Naida CI Q30 CI-5260-120

  IMPLANT, COCHLEAR
  1 recall0 reports
• Naida CI Q30 CI-5260-150

  IMPLANT, COCHLEAR
  1 recall0 reports

Other Advanced Bionics, LLC products

• Naida CI Q703 models · 0 reports · 1 recall