GN ReSound 20967272Recalls & reported problems

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 05708296156801), received between Dec 28, 2020 and Dec 28, 2020 — classified as 1 injury.

The most frequently reported specific device problem is “Device-Device Incompatibility” (1 report).

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 16, 2026.

Most reported problems

Recent adverse event reports

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

• InjuryDec 28, 2020Device-Device Incompatibility; Device-Device Incompatibility

  AS REPORTED BY LOCAL CUSTOMER SERVICE: LOUD SCREECHING SOUND AFTER GETTING THE LOW BATTERY INDICATOR. GETS A "LOUD SCREECHING SOUND" AFTER 10-15 MINUTES AFTER GETTING THE LOW BATTERY WARNING. IF YOU OPEN AND THEN CLOSE THE BATTERY DOOR THE AID IS "DEAD" AND HE WILL THEN REPLACE THE BATTERY AND THEN IT WORKS FINE. PATIENT EXPERIENCING BAD TINNITUS FROM SCREECH AND RIGHT EAR HURTS FROM SCREECH. QUESTIONNAIRE: WAS THE SOUND PAINFUL AND/OR DID IT CAUSE HARM TO THE PATIENT OR OTHER PERSON? YES HAS THE PATIENT BEEN IN CONTACT WITH A PROFESSIONAL? NO. PLEASE CHOOSE THE DURATION OF THE SOUND? UP TO 10 SECONDS WHAT TYPE OF RECEIVER? MEDIUM POWER. FINAL REPORT SUMMARY AND CONCLUSION.

  Patient problems: Partial Hearing Loss; Skin Irritation

  MAUDE report 11075372 ↗