Model Number CI24RE (L24) |
Device Problem
Appropriate Term/Code Not Available (3191)
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Patient Problem
Patient Problem/Medical Problem (2688)
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Event Date 01/17/2017 |
Event Type
Injury
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Manufacturer Narrative
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This report is submitted on (b)(6) 2017, by (b)(4).
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Event Description
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Per the clinic, the device was explanted on (b)(6) 2017, due to a loss of residual hearing resulting in a lack of benefit with the hybrid device.The patient was reimplanted with another cochlear device during the same surgery.
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Manufacturer Narrative
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Correction: the correct "explanted date" is (b)(6) 2017, not (b)(6) 2017, as initially reported.
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Manufacturer Narrative
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This report is submitted on april 21, 2017.
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Search Alerts/Recalls
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