GN ReSound 21593800Recalls & reported problems

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 05708296200634), received between Jun 23, 2023 and Jun 23, 2023 — classified as 1 malfunction.

The most frequently reported specific device problem is “Overheating of Device” (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.

• MalfunctionJun 23, 2023Overheating of Device; Overheating of Device

  26MAY2023 IT WAS REPORTED: MEMBER BROUGHT PREZA CHARGER INTO STORE YESTERDAY STATING IT 'BLEW UP'. CLARIFIED THAT CHARGER MADE A SOUND WHEN PLUGGED IN AND BURNT AT PORT WHERE CHARGER AND CORD MEET. SHE UNPLUGGED CHARGER AND PROMPTLY BROUGHT INTO THE STORE. NO HARM TO PEOPLE OR PROPERTY. DEVICE IS OUT OF WARRANTY, HOWEVER EXTENDED COURTESY REPLACEMENT. PROVIDER GAVE HER A LOANER CHARGER/CORD AND TOLD HER TO TOSS THE CORD THAT IS AT HOME.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 17189609 ↗