GN ReSound 20686220Recalls & reported problems

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 05708296145447), received between Dec 28, 2020 and Dec 28, 2020 — classified as 1 malfunction.

The most frequently reported specific device problem is “Charging Problem” (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.

• MalfunctionDec 28, 2020Charging Problem; Charging Problem

  AS REPORTED BY LOCAL CUSTOMER SERVICE: AID HOT TO THE TOUCH AND NOT HOLDING CHARGE. I HAVE A PATIENT WANTING TO BRING HER AIDS IN TOMORROW. SHE HAS HAD THE QUATTRO 7 SINCE SEPTEMBER AND NOW WHEN SHE REMOVES THEM ONE IS DEAD AND THE OTHER IS HOT! I TOLD HER NOT TO WEAR THEM AND TO BRING THEM IN IMMEDIATELY WITH THE CHARGER SO I CAN SEND THEM IN. WOULD IT BE POSSIBLE FOR YOU TO SEND ANOTHER SET OVERNIGHT? I KNOW THEY USUALLY DON'T REPAIR THEM WHEN THIS HAPPENS. HERE ARE HER SERIAL NUMBERS: (B)(6) & (B)(6) . QUESTIONNAIRE: DID THE EVENT AND/OR DEVICE CAUSE HARM TO THE PATIENT, OTHER PERSON(S) OR PROPERTY? NO PREVIOUSLY AN INITIAL REPORT HAS BEEN SENT - THIS IS THE FOLLOW-UP/FINAL REPORT.

  Patient problems: Skin Irritation; Superficial (First Degree) Burn

  MAUDE report 11075547 ↗