Platinum Series Headpiece Model Number AB-7300. The… recallZ-0957-2009 · Advanced Bionics LLC · initiated Jul 24, 2008
Terminated All recalls posted in February 2009
Is my device affected?
- Compare the model, catalog and lot or serial numbers on your device or its packaging with the code information below. A recall usually covers only specific models or lots.
- If yours is listed, follow the instructions from Advanced Bionics LLC or your healthcare provider. The company's action is summarized under what the company is doing.
- Do not stop using a prescribed or implanted device on your own — talk to your healthcare provider first.
Where to find your model and lot numbers · What recall classes and statuses mean
Why it was recalled
Mistuned headpiece - Advanced Bionics recently became aware of a tuning issue with some Platinum Series and S-Series headpieces shipped from May 2007 through April 2008. Tuning refers to the process through which the headpiece's communication frequency is adjusted to match that of the internal device. Potential clinical symptoms include: -No lock -Intermittent lock -Implant locks, but can
FDA root cause category: Employee error
What the company is doing
Advanced Bionics is notifying clinicians of this situation so that they can provide appropriate clinical management. The notification letter sent to clinicians in the United States was sent via FedEx so that delivery information could be confirmed. The letter advises that Advanced Bionics recently became aware of a tuning issue with some Platinum Series and S-Series headpieces shipped from May 2007 through April 2008. Auria and Harmony headpieces are not affected by this issue. Tuning refers to the process through which the headpiece's communication frequency is adjusted to match that of the internal device. Since discovery of this issue firm has conducted an extensive technical analysis showing that the use of these headpieces does not pose any safety risk to the patient. While there has been no increase in the number of headpiece-related complaints, firm advises of the potential clinical symptoms: -No lock -Intermittent lock -Implant locks, but cannot measure impedances -Reduction in battery life, primarily for C1 patients with thick flaps. Per the letter, as long as the system maintains lock, there is no degradation in sound quality or stimulation. Further, the impact on battery life for CII and HiRes 90K patients is minimal. Medical professionals are advised that If they have any patients who display any of these clinical symptoms that they attribute to an affected headpiece, to advise the patient to contact Advanced Bionics Customer Service at 877-244-9541 and they will send them a replacement promptly.
Recall details
- Recall number
- Z-0957-2009
- Recall class
- Not yet classified by the FDA
- Status
- Terminated
- Initiated by the company
- Jul 24, 2008
- Posted by the FDA
- Feb 3, 2009
- Recalling firm
- Advanced Bionics LLC
- Quantity
- 2,123 units
- Product code
- MCM
- FDA submissions
- P960058
- Distribution
- Nationwide
Product description
Platinum Series Headpiece Model Number AB-7300. The headpiece is used in conjunction with speech processors manufactured by Advanced Bionics. The Harmony HiResolution Bionic Ear System and Clarion Multi-Strategy Cochlear Implant are cochlear implant systems designed to provide useful hearing to individuals with severe-to-profound sensorineural hearing loss
Code information (models, lots, serial numbers)
Show the full code information (15k characters)
Model #AB-7300; Serial Numbers: 36241, 36242, 36243, 36244, 36245, 36246, 36247, 36248, 36249, 36250, 36251, 36252, 36253, 36254, 36255, 36256, 36257, 36258, 36259, 36260, 36261, 36262, 36263, 36264, 36265, 36266, 36267, 36268, 36269, 36270, 36271, 36272, 36273, 36274, 36275, 36276, 36291, 36292, 36293, 36295, 36297, 36298, 36299, 36300, 36324, 36325, 36326, 36327, 36328, 36329, 36330, 36331, 36332, 36333, 36334, 36335, 36336, 36338, 36339, 36340, 36341, 36342, 36343, 36344, 36345, 36346, 36347, 36348, 36349, 36350, 36351, 36352, 36353, 36354, 36355, 36356, 36357, 36358, 36359, 36360, 36481, 36482, 36483, 36484 36485, 36486, 36487, 36488, 36489, 36490, 36491, 36493, 36494, 36495, 36496, 36497, 36498, 36499, 36500, 36501, 36502, 36503, 36504, 36506, 36507, 36508, 36509, 36510, 36511, 36512, 36513, 36514, 36515 36516, 36517, 36518, 36519, 36520, 36521, 36522, 36523, 36524, 36525, 36526, 36527, 36528, 36529 36530, 36531, 36532, 36533, 36534, 36535, 36536, 36537, 36538, 36539, 36540, 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Other devices under the same FDA submission
25 devices cleared under P960058 — the recall does not name any of them by identifier. One submission often covers many models, so they may or may not be affected.
- HiRes™ Ultra CI HiFocus™ MS Electrode CI-1600-04Advanced Bionics AG · Implant, Cochlear2,918 reports
- HiRes™ Ultra 3D CI HiFocus™ MS Electrode CI-1601-04Advanced Bionics AG · Implant, Cochlear1 death931 reports
- HiRes™ Ultra 3D CI HiFocus™ SlimJ Electrode CI-1601-05Advanced Bionics AG · Implant, Cochlear795 reports
- HiRes™ Ultra CI HiFocus™ SlimJ Electrode CI-1600-05Advanced Bionics AG · Implant, Cochlear335 reports
- HiRes 90K™ Advantage CI HiFocus™ MS Electrode CI-1500-04Advanced Bionics AG · Implant, Cochlear315 reports
- HiRes 90K™ Advantage CI HiFocus™ 1j Electrode CI-1500-01Advanced Bionics AG · Implant, Cochlear280 reports
- HiRes™ Ultra 3D CI HiFocus™ SlimJ Electrode CI-1601-05Advanced Bionics, LLC · Implant, cochlear1 death257 reports
- HiRes™ Ultra 3D CI HiFocus™ SlimJ Electrode CI-1601-05Advanced Bionics AG · Implant, Cochlear254 reports
- HiRes™ Ultra 3D CI HiFocus™ MS Electrode CI-1601-04Advanced Bionics, LLC · Implant, cochlear1 recall149 reports
- HiRes™ Ultra 3D CI HiFocus™ MS Electrode CI-1601-04Advanced Bionics AG · Implant, Cochlear195 reports
- HiRes™ Ultra CI HiFocus™ SlimJ Electrode CI-1600-05Advanced Bionics AG · Implant, Cochlear178 reports
- HiRes 90K™ Advantage CI HiFocus™ MS Electrode CI-1500-04Advanced Bionics AG · Implant, Cochlear1 recall127 reports
Other products in the same recall event
The FDA groups related products into one recall event (event 50204).
- Z-0956-2009 · TerminatedHR90K Platinum Series Headpiece Model Number AB-7300-001 ADVANCED BIONICS LLC 12740 San Fernando Rd. Sylmar, CA 91342 USA. The HiRes90K headpiece is used in conjunction with spee…
- Z-0958-2009 · TerminatedS-Series Long Range Headpiece Model Number AB-5301-00 (beige) and AB-5301-10 (brown) ADVANCED BIONICS LLC 12740 San Fernando Rd. Sylmar, CA 91342 USA. The headpiece is used in …
- Z-0959-2009 · TerminatedS-Series Short Range Headpiece Model Number MMT-5300-00 (beige) and MMT-5300-10 (brown) ADVANCED BIONICS LLC 12740 San Fernando Rd. Sylmar, CA 91342 USA. The headpiece is used i…
Sources and updates
- Recall record: FDA Medical Device Recalls, file dated Oct 16, 2026 · View the FDA recall notice ↗
- Devices: FDA GUDID, file dated Oct 13, 2026. Devices are linked when their identifier (with a valid check digit) appears in the recall's code information.
- Page last rebuilt: Oct 18, 2026. Text above is shown as published by the FDA.
How recalls are matched to devices · Editorial policy · Report an error on this page