HiRes™ Ultra CI HiFocus™ MS Electrode CI-1600-04 (UDI 07630016877971)Recalls & reported problems
Advanced Bionics AG · Class 3 · Implant
All models of HiRes Ultra CI HiFocus MS Electrode (2)
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 1
- Deaths reported
- 0
- Injuries reported
- 1
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 07630016877971), received between Apr 5, 2022 and Apr 5, 2022 — classified as 1 injury.
17 other recalls cover devices cleared under the same FDA submission (P960058); they may or may not involve this specific model.
Reports come from manufacturers, hospitals and patients and are not verified by the FDA. A report does not prove the device caused the event, and counts can't be used to compare devices or estimate failure rates. What reports can and can't tell you · How this data works · Data updated Oct 18, 2026.
Most reported problems
Device problems
- Adverse Event Without Identified Device or Use Problem1
- Appropriate Device Problem Term/Code Not Available1
Patient problems
- Unspecified Infection1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
InjuryApr 5, 2022Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem; Appropriate Device Problem Term/Code Not Available
THE RECIPIENT REPORTEDLY EXPERIENCED OPEN ELECTRODES. ON (B)(6) 2021, THE RECIPIENT UNDERWENT REPOSITIONING SURGERY UPON WHICH AN INFECTION WAS DISCOVERED. THE ELECTRODE COULD NOT BE REINSERTED AND WAS LEFT IN THE MASTOID DUE TO THE INFECTION. THE RECIPIENT WAS REPORTEDLY TREATED WITH ANTIBIOTICS (TYPE UNKNOWN). ON (B)(6) 2022, REINSERTION SURGERY WAS ATTEMPTED, HOWEVER IT WAS UNSUCCESSFUL AS THE ELECTRODE WAS ENCASED WITH FIBROUS AND BONY TISSUE. THE RECIPIENT'S DEVICE WAS EXPLANTED. THE RECIPIENT WAS REIMPLANTED WITH ANOTHER ADVANCED BIONICS COCHLEAR DEVICE.
Patient problems: Unspecified Infection
MAUDE report 14014846 ↗
Recalls under the same FDA submission
These recalls involve devices cleared under P960058. One submission often covers many models, so check the product and lot details in each record.
- Z-2283-2026 · Apr 30, 2026 · Open, ClassifiedBrand Name: HiResolution" Bionic Ear System Product Name: HiRes Ultra 3D CI HiFocus Mid Scala Model/Catalog Number: CI-1601-04 Software Version: N/A Product Description: The HiReso
- Z-1950-2026 · Mar 23, 2026 · Open, ClassifiedBrand Name: HiResolution" Bionic Ear System Product Name: M Zn-Air Battery Pak Model/Catalog Number: CI-5501-110; CI-5501-120; CI-5501-130; CI-5501-140; CI-5501-150; CI-5501-190; C
- Z-1813-2025 · Mar 5, 2025 · Open, ClassifiedHiResolution" Bionic Ear System - M Battery Charger Model Number CI-5607
- Z-2033-2020 · Feb 17, 2020 · TerminatedAB 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 sensorine
- Z-2032-2020 · Feb 17, 2020 · TerminatedAB HiResolution Bionic Ear System, HiRes Ultra 3D CI, HiFocus SlimJ Electrode - Product Usage: The device is intended to restore a level of auditory sensation to patients with prof
- Z-1441-2020 · Apr 4, 2019 · TerminatedSoundWave Professional Suite Software 3.2, Ref CI-6055-014, SPN 058-023-32085, UDI: (01)07630016853227, Logical SoundWave Professional Suite 3.2, CE 0123 - Product Usage: Soundwave
- Z-1259-2020 · Mar 18, 2019 · TerminatedHiResolution Bionic Ear System HiRes 90K Advantage CI HiFocus MS Electrode REF CI-1500-04. Cochlear Implant.
- Z-1085-2019 · Feb 6, 2019 · TerminatedNada CI Q90 Sound Processor, Silver Gray, Model Cl-5280-140.
- Z-1084-2019 · Feb 6, 2019 · TerminatedNada CI Q70 Sound Processor, Sand Beige, Model Cl-5245-120; Silver Gray, Model Cl-5245-140; and Velvet Black, Model Cl-5245-150.
- Z-1083-2019 · Feb 6, 2019 · TerminatedNada CL Q30 Sound Processor, Sand Beige, Model Cl-5260-120; Silver Gray, Model Cl-5260-140; and Velvet Black, Model Cl-5260-150.
- Z-2039-2009 · Jun 10, 2009 · TerminatedAdvanced 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
- Z-0958-2009 · Jul 24, 2008 · 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 · Jul 24, 2008 · 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
- Z-0956-2009 · Jul 24, 2008 · 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-0957-2009 · Jul 24, 2008 · TerminatedPlatinum Series Headpiece Model Number AB-7300. The headpiece is used in conjunction with speech processors manufactured by Advanced Bionics. The Harmony HiResolution Bionic Ear
…and 2 more.
Other Implant, Cochlear devices
- HiRes™ Ultra CI HiFocus™ MS Electrode CI-1600-04Advanced Bionics AG · Implant, Cochlear2,918 reports
- Cochlear® Nucleus® CI512 cochlear ImplantCochlear Limited · IMPLANT, COCHLEAR2,771 reports
- Cochlear® Nucleus® CI622 cochlear Implant with Slim Straight electrodeCochlear Limited · Implant, cochlear2,115 reports
- Cochlear® Nucleus® CI632 cochlear Implant with Slim Modiolar electrodeCochlear Limited · Implant, cochlear2,057 reports
- Nucleus Z60353Cochlear Limited · IMPLANT, COCHLEAR2 deaths1,815 reports
- Cochlear® Nucleus® CI522 cochlear Implant with Slim Straight electrodeCochlear Limited · IMPLANT, COCHLEAR1,475 reports
- Cochlear® Nucleus® CI612 cochlear ImplantCochlear Limited · Implant, cochlear1,150 reports
- Nucleus Z190574Cochlear Limited · IMPLANT, COCHLEAR981 reports
Sources and updates
- Device record: FDA GUDID, file dated Oct 13, 2026 · View this device in AccessGUDID ↗
- Adverse event reports: FDA MAUDE, file dated Oct 14, 2026 · each report above links to its original FDA record
- Recalls: FDA Medical Device Recalls, file dated Oct 16, 2026
- Page last rebuilt: Oct 18, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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