FDA Adverse Event Malfunction Summary report: N

GN RESOUND

MDR report key: 16644436 · Received March 30, 2023

Report

Report Number
3005650109-2023-00040
Event Type
Malfunction
Date Received
March 30, 2023
Date of Event
March 1, 2023
Report Date
April 28, 2023
Manufacturer
GN HEARING A/S
Product Code
OSM
UDI-DI
05708296147113
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
SN
Reporter Occupation
OTHER HEALTH CARE PROFESSIONAL
Health Professional
Yes

Narratives

Additional Manufacturer Narrative · 0

MANUFACTURER'S REF# (B)(4). INVESTIGATION IS STILL IN PROGRESS; A FINAL REPORT WILL BE SUBMITTED UPON COMPLETION. 28 APRIL 2023: TECHNICAL INVESTIGATION CONCLUDED: DEVICE INVESTIGATION CONCLUDED: THE DEVICE IN QUESTION, AN APOLLO 5.1 C-1 CHARGER SHOWED SIGNS OF DEFORMATION AND OVERHEATING INSIDE THE MICRO USB CONNECTOR. A LOW OHMIC CONNECTION HAD APPEARED BETWEEN VBUS AND THE GROUNDED METAL HOUSING INSIDE THE CABLE CONNECTOR. THE MICRO USB CONNECTOR IN THE APOLLO 5.1 HAS MECHANICAL LIMITATIONS, IF IT IS SUBJECTED TO 'ROUGH' HANDLING BY THE USER. THE MECHANICAL SUPPORT (CHARGER PLASTIC HOUSING) CANNOT MITIGATE THE DEFORMATION OF THE CONNECTOR. WHEN THAT HAPPENS, IT IS OPEN FOR WRONG INSERTIONS OF THE CONNECTOR. THE PINS OF THE FEMALE USB CONNECTOR APPEARS TO BEND DOWNWARDS, WHICH CAN CREATE A NON-IDEAL CONNECTION WHEN THE CABLE CONNECTOR IS INSERTED. A DHR REVIEW HAVE BEEN COMPLETED. NO DEVIATION OR CHANGES WERE FOUND DURING MANUFACTURING OF THE DEVICE. CLINICAL ASSESSMENT CONCLUDED: CLINICAL EVALUATION OF THE EVENT: THE CASE INVOLVES A MICRO CHARGER PORT AND WIRE OVERHEATED. NO INFORMATION RECEIVED ON THE ACTIONS LEADING TO THIS EVENT. NO PATIENT HARM OR PROPERTY DAMAGE REPORTED. IT IS UNKNOWN IF THE ORIGINAL EQUIPMENT WAS USED. BASED ON THE RESULT FROM R&D INVESTIGATION OF THE ACTUAL DEVICE, CLINICAL CONCLUSION ON THE CASE IS THAT THERE IS A POTENTIAL RISK OF HEAT DISSIPATION BASED ON THE FINDINGS. A LOW OHMIC CONNECTION HAD APPEARED BETWEEN VBUS AND THE GROUNDED METAL HOUSING INSIDE THE CABLE CONNECTOR. A DAMAGED POWER SUPPLY OR A POWER SUPPLY OF VERY POOR QUALITY COULD LEAD TO BURN INJURIES AND IN RARE CONDITIONS THERE IS A SMALL RISK THAT A WRONG CHARGING OR DISCHARGING OR A BATTERY THERMAL RUNWAY CAN LEAD TO HIGH TEMPERATURES OR FIRE ACCIDENTS. THE CHARGERS HAVE BEEN TESTED ACCORDING TO APPLICABLE SAFETY STANDARDS. THESE RISKS ARE REDUCED AS FAR AS POSSIBLE AND THE PROBABILITY OF OCCURRENCE OF THESE EVENTS IS CONSIDERED VERY LOW. THERE ARE NO NEW CLINICAL ASPECTS (E.G. UNFORESEEN USE OR CLINICAL CONDITIONS) DISCOVERED FROM THIS EVENT. THEREFORE, IT IS CONCLUDED THAT THE CURRENT CLINICAL EVALUATION AND RISK/BENEFIT CONCLUSION HEREIN ARE SUFFICIENT. RISK ASSESSMENT CONCLUDED: THE RESIDUAL RISK AFTER THE RISK CONTROL MEASURE(S) IS ACCEPTABLE. NO NEW HAZARDOUS SITUATIONS REVEALED AND NO NEED TO UPDATE THE RISK REGISTER. MANUFACTURER'S INVESTIGATION IS FINAL. THIS IS A FINAL REPORT.

Additional Manufacturer Narrative · 0

MANUFACTURER'S REF# (B)(4). INVESTIGATION IS STILL IN PROGRESS; A FINAL REPORT WILL BE SUBMITTED UPON COMPLETION.

Description of Event or Problem · 0

ON (B)(6) 2023, PATIENT FOUND CHARGER BURNED AT THE CHARGER USB SLOT AND CABLE AT HOME. NO REPORTS OF PATIENT HARM OR INJURY AND NO MEDICAL INTERVENTION WAS REQUIRED. NO DAMAGE TO PROPERTIES IS REPORTED. UNKNOWN WHETHER ORIGINAL EQUIPMENT WAS USED. DEVICE HAS BEEN REQUESTED BACK FOR FURTHER INVESTIGATION.

Description of Event or Problem · 0

ON (B)(6) 2023, PATIENT FOUND CHARGER BURNED AT THE CHARGER USB SLOT AND CABLE AT HOME. NO REPORTS OF PATIENT HARM OR INJURY AND NO MEDICAL INTERVENTION WAS REQUIRED. NO DAMAGE TO PROPERTIES IS REPORTED. UNKNOWN WHETHER ORIGINAL EQUIPMENT WAS USED. DEVICE HAS BEEN REQUESTED BACK FOR FURTHER INVESTIGATION.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
591481 GN RESOUND HEARING AID, AIR CONDUCTION WITH WIRELESS TECHNOLOGY OSM GN HEARING A/S 20472100 05708296147113

Patients

Seq Age Sex Outcome Treatment
1 56 YR Female