FDA Recall Terminated

Advanced Bionics HiRes 90K Cochlear Implant, Model: CI-1400-01 and CI-1400-02H, Implant Magnet Case. Cochlear implant intended to restore a level of auditory sensation to patients with profound sensorineural deafness via electrical stimulation of the auditory nerve.

Recall: Z-2039-2009 · Initiated June 10, 2009

Recall

Recall Number
Z-2039-2009
Event Number
52700
Firm
Advanced Bionics LLC
FEI Number
3006556115
Product Code
MCM
Status
Terminated
Root Cause
Process control
Initiated
June 10, 2009
Posted
September 11, 2009
Terminated
March 26, 2012
Address
12740 San Fernando Rd, Sylmar, CA, 91342-3728

Description

Advanced Bionics HiRes 90K Cochlear Implant, Model: CI-1400-01 and CI-1400-02H, Implant Magnet Case. Cochlear implant intended to restore a level of auditory sensation to patients with profound sensorineural deafness via electrical stimulation of the auditory nerve.

Reason

The recall was initiated after Advanced Bionics became aware of fourteen (14) devices manufactured between May 27, 2005 and June 30, 2005 that are confirmed to have or potentially have an issue related to the internal magnet. These devices are were made with an internal magnet where the metal case surrounding the magnet was not properly welded. Patients with these devices may experience a decreas

Action

Advanced Bionics, LLC issued an "Important Notification" dated June 10, 2009 via Fed Ex to Consignees in the US and Canada. Outside of the US, the notification letters will be distributed in such a manner that delivery confirmation can be obtained. There were three type of notification letters distributed: one for Patients, one for Surgeons and one for Clinicians. Letters described the affected device prompting users on what to do next. An acknowledgement form was enclosed and should be completed and sent via fax to 1-661-362-7621. For further information, contact Advanced Bionics at 1-877-829-0026.

Distribution

Worldwide Distribution -- US, Canada, France and South Korea.

Quantity

18