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Baha 92841Recalls & reported problems

Cochlear Bone Anchored Solutions AB · Baha BP110 Power, Soft Black · Class 2

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 09321502021142), received between Feb 22, 2018 and Feb 22, 2018 — classified as 1 injury.

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. How this data works · Data updated Oct 13, 2026.

Most reported problems

Device problems

  • Appropriate Device Problem Term/Code Not Available1

Patient problems

  • Pain1
  • Patient Problem/Medical Problem1
  • Scarring1

Recent adverse event reports

The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.

  • InjuryFeb 22, 2018Appropriate Device Problem Term/Code Not Available; Appropriate Device Problem Term/Code Not Available

    PER THE CLINIC, THE PATIENT EXPERIENCED SCARRING AND PAIN AT THE ABUTMENT SITE. SUBSEQUENTLY, THE PATIENT WAS TREATED WITH MEDICATION (TYPE AND DATE NOT REPORTED). IT WAS ALSO REPORTED THE SKIN ISSUE IS PERSISTENT.

    Patient problems: Pain; Patient Problem/Medical Problem; Scarring

    MAUDE report 7288132 ↗

Other Hearing aid, bone conduction devices

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Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.