Adverse Event Report from FDA on HiRes90k
August 6, 2008 · Print This Article
The Food and Drug Administration (FDA) issued an Adverse Event report for the Advanced Bionics Clarion HiRes90k cochlear implant. As stated in the Report:
| Date FDA Received | 05/19/2006 |
|---|---|
| Is This An Adverse Event Report? | Yes |
| Is This A Product Problem Report? | Yes |
| Device Operator | Lay User/Patient |
| Device MODEL Number | HIRES90K |
| Was Device Available For Evaluation? | Device Returned To Manufacturer |
| Date Returned to Manufacturer | 05/19/2006 |
| Is the Device an Implant? | Yes |
You can visit the FDA’s website and read the report by clicking HERE.
If you believe you have been physically or emotionally injured as a result of the Advanced Bionics clarion HiRes90k cochlear implant, please call Tim Edwards or Ed Wallis at (901) 527-4673, or SEND US AN E-MAIL today.
You can also click HERE for more information.
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