FDA Adverse Event Malfunction Summary report: N

HAMILTON MEDICAL AG

MDR report key: 17681649 · Received September 5, 2023

Report

Report Number
3001421318-2023-14545
Event Type
Malfunction
Date Received
September 5, 2023
Date of Event
April 24, 2022
Report Date
September 1, 2023
Manufacturer
HAMILTON MEDICAL AG
Product Code
CBK
UDI-DI
00730002856789
PMA / PMN Number
K193228
Product Problem
Yes
Report Source
Manufacturer report
Reporter Occupation
OTHER HEALTH CARE PROFESSIONAL
Health Professional
Yes

Narratives

Additional Manufacturer Narrative · 0

SINCE THE COMPLAINT IN QUESTION WAS SUBMITTED TO HAMILTON MEDICAL AG MORE THAN 2 YEARS AGO, NO ATTEMPTS WILL BE PERFORMED TO OBTAIN ADDITIONAL INFORMATION. NO FURTHER INVESTIGATION OR CORRECTION WILL BE PERFORMED EXCEPT THOSE MENTIONED ABOVE. IN FUTURE HAMILTON MEDICAL AG WILL REPORT AN EVENT SIMILAR TO THIS ISSUE AS IT WILL BE DEEMED A REPORTABLE EVENT. THE ALLEGATION IN THIS COMPLAINT WAS CONFIRMED TO BE A COMPLAINT. WITH THIS INVESTIGATION IT HAS BEEN CONFIRMED THAT THE DEVICE FAILED TO MEET ITS SPECIFICATIONS AT THE TIME OF THE EVENT WHILE THE VENTILATOR WAS USED. THE ROOT CAUSE WAS DETERMINED TO BE A DEFECTIVE G5 VU MOTHER BOARD. IN CONSEQUENCE (CORRECTION) THE DEFECTIVE G5 VU MOTHER BOARD WAS REPLACED. THERE WAS NO PATIENT OR USER HARM.

Description of Event or Problem · 0

TF 9907 MESSAGE FROM (B)(6): I RECEIVED A CALL FROM (B)(6) FROM UC HEALTH LOCATED IN (B)(6). (B)(6) INFORMS ME THAT ONE OF OUR HAMILTON-G5 UNITS EXPERIENCED A FAILURE DURING A NEONATAL PATIENT TREATMENT. THE ERROR CODE OBSERVED BY STAFF IS TF9907. AT THIS TIME, NO PATIENT FATALITY IS REPORTED, AND THEY WERE ABLE TO SUCCESSFULLY TRANFER THE PATIENT TO A DIFFERENT VENTILATOR. ACCORDING TO OUR MANUALS, THIS IS RELATED TO A CONNECTION ISSUE BETWEEN THE IPP AND THE VU.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1006305 HAMILTON MEDICAL AG HAMILTON-G5 CBK HAMILTON MEDICAL AG HAMILTON-G5 00730002856789

Patients

Seq Age Sex Outcome Treatment
1 Unknown