GN Hearing EP2CIC-LPRecalls & reported problems

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 05708296345557), received between Mar 21, 2025 and Mar 21, 2025 — classified as 1 malfunction.

The most frequently reported specific device problem is “Defective Component” (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. How this data works · Data updated Oct 13, 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.

• MalfunctionMar 21, 2025Defective Component; Defective Component

  ESTIMATED DATE OF INCIDENT 20FEB2025. IT WAS REPORTED THE FILTER GROMMET IS LOSE ON AN IN THE EAR HEARING AID. THERE IS NO ALLEGATION OF HARM TO THE USER. THERE IS NO FURTHER INFORMATION ON THE CASE. FURTHER FOLLOW UP IS EXPECTED. 15APR2025 NO FURTHER FOLLOW UP HAS BEEN RECEIVED.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 21663052 ↗