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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, Classified
    Brand 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, Classified
    Brand 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, Classified
    HiResolution" Bionic Ear System - M Battery Charger Model Number CI-5607
  • Z-2033-2020 · Feb 17, 2020 · Terminated
    AB 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 · Terminated
    AB 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 · Terminated
    SoundWave 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 · Terminated
    HiResolution Bionic Ear System HiRes 90K Advantage CI HiFocus MS Electrode REF CI-1500-04. Cochlear Implant.
  • Z-1085-2019 · Feb 6, 2019 · Terminated
    Nada CI Q90 Sound Processor, Silver Gray, Model Cl-5280-140.
  • Z-1084-2019 · Feb 6, 2019 · Terminated
    Nada 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 · Terminated
    Nada 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 · 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
  • Z-0958-2009 · Jul 24, 2008 · Terminated
    S-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 · Terminated
    S-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 · Terminated
    HR90K 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 · Terminated
    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

…and 2 more.

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Sources and updates

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