FDA Adverse Event Malfunction Summary report: N

HAMILTON MEDICAL AG

MDR report key: 18462001 · Received January 8, 2024

Report

Report Number
3001421318-2023-26415
Event Type
Malfunction
Date Received
January 8, 2024
Date of Event
October 2, 2020
Report Date
January 5, 2024
Manufacturer
HAMILTON MEDICAL AG
Product Code
CBK
UDI-DI
00730002856789
PMA / PMN Number
K153046
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
PL
Reporter Occupation
OTHER HEALTH CARE PROFESSIONAL
Health Professional
Yes

Narratives

Additional Manufacturer Narrative · 0

THE COMPLAINT HAS BEEN REOPENED AND REVIEWED ACCORDING TO FDA FORM 483 INSPECTIONAL OBSERVATION EMS #2, EOBS2 FROM THE FDA INSPECTION CONDUCTED BETWEEN JULY 17 TO JULY 21, 2022 AT THE EMS AND BONADUZ SITES. A DETAILED INVESTIGATION WAS PERFORMED BY AN EXPERT FROM THE TECHNICAL SERVICE: SINCE THE COMPLAINT IN QUESTION WAS SUBMITTED TO HAMILTON MEDICAL AG OVER 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. THE ROOT CAUSE WAS DETERMINED TO BE DEFECTIVE COMPONENTS OF THE VENTILATOR. IT COULD NOT BE DETERMINED MORE SPECIFICALLY. IN CONSEQUENCE THE COMPONENTS WERE REPLACED. THERE WAS NO PATIENT OR USER HARM.

Description of Event or Problem · 0

FAN FAILURE - YELLOW ALARM. THE FAN NO ROTARY. I CHECKED IT IN C-1, NO EFFECT. I CAN'T UPDATE TESLASPY BOARD. TESLASPY WORK CORRECTLY, BUT MIUPDATER SHOW MESSAGE - NO COMMUNICATION.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
620926 HAMILTON MEDICAL AG HAMILTON-MR1 CBK HAMILTON MEDICAL AG HAMILTON-MR1 00730002856789

Patients

Seq Age Sex Outcome Treatment
1 Unknown