Beltone RLY3ITC-DW-MPRecalls & reported problems

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 05708296208142), received between Apr 19, 2023 and Apr 19, 2023 — classified as 1 injury.

The most frequently reported specific device problem is “Product Quality 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 18, 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.

• InjuryApr 19, 2023Product Quality Problem; Product Quality Problem

  (B)(6) 2023: IT HAS BEEN REPORTED THAT WAX FILTERS IN THE HEARING AID HAVE FALLEN OFF IN USER'S EARS. THE USER HAD TO GO TO HOSPITAL TO GET THEM REMOVED. THE WHITE RING CASING THAT HOUSES THE WAX FILTER LOOKS TO BE CRACKED. THE WAX FILTERS DO NOT SIT NEATLY, THEY PROTRUDE MORE THAN NORMAL AND DON'T SIT SYMMETRICALLY FLAT.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 16766826 ↗