FDAFebruary 17, 2020device

AB HiResolution Bionic Ear System, HiRes Ultra CI, MS Electrode - Product Usage: The device is intended to restore a level of auditory sensation to patients with profound sensorineural deafness via electrical stimulation of the auditory nerve.

Official recall recorded by the U.S. Food & Drug Administration.

The hazard

hearing performance degradation due to body-fluid entering the device.

What to do

FDA enforcement status: Terminated

Brands named

advanced bionicsadvanced

Recall history

Other federal recalls tied to the same brand — a factual pattern, straight from the source data.

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