FDA Adverse Event Malfunction Summary report: N

STARKEY EVOLV AI HEARING AIDS

MDR report key: 17010723 · Received May 25, 2023

Report

Report Number
MW5117911
Event Type
Malfunction
Date Received
May 25, 2023
Date of Event
February 13, 2023
Report Date
May 5, 2023
Manufacturer
STARKEY LABORATORIES, INC.
Product Code
ESD
Product Problem
Yes
Report Source
Voluntary report
Reporter Location
OK, US
Reporter Occupation
PATIENT
Health Professional
N

Narratives

Description of Event or Problem · 0

PATIENT CALLED TO REPORT THAT HIS STARKEY HEARINGS AIDS ARE UNSATISFACTORY DUE TO CONSISTENT BACKGROUND NOISE AND FAILURE OF HIS PROVIDER TO FOLLOW UP FOR PROPER SET-UP AND ADJUSTMENTS. PATIENT LEARNED THAT HE WAS GIVEN THE WRONG HEARING AIDS BY STARKEY AND WAS TOLD THAT THEY WOULD BE REPLACED FOR THE CORRECT HEARING AIDS BUT HAVE NOT HEARD BACK FROM THEM. HE PAID (B)(6) FOR THE HEARING AIDS AND HAS ATTEMPTED TO CONTACT HIS PROVIDER BUT HAS NOT HEARD BACK FROM THEM AND HIS INSURANCE COMPANY. STARKEY WILL NOT REIMBURSE HIM FOR THE DEVICES. PATIENT STATES THAT HE WOULD KEEP THE HEARING AIDS IF HE CAN GET A FOLLOW-UP APPOINTMENT FOR PROPER CARE, SET-UP AND ADJUSTMENTS.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
650210 STARKEY EVOLV AI HEARING AIDS HEARING AID, AIR-CONDUCTION, PRESCRIPTION ESD STARKEY LABORATORIES, INC. AI 2400

Patients

Seq Age Sex Outcome Treatment
1 56 YR Male