FDA Adverse Event Death Summary report: N

HAMILTON-C1

MDR report key: 18615802 · Received January 31, 2024

Report

Report Number
3016723884-2024-00004
Event Type
Death
Date Received
January 31, 2024
Date of Event
January 10, 2024
Report Date
January 31, 2024
Manufacturer
HAMILTON MEDCIAL AG
Product Code
CBK
UDI-DI
07630002800747
Adverse Event
Yes
Report Source
Distributor report
Reporter Location
NV, US
Reporter Occupation
OTHER

Narratives

Description of Event or Problem · 0

ALERTS WITH "DISCONNECTION ON PATIENT SIDE" AND "MAXIMUM LEAK COMPENSATION" BIOMED SAYS THAT HOSPITAL STAFF WAS GETTING LOTS OF DISCONNECTION ALARMS. HE SAYS THAT THE PATIENT HAS PASSED AWAY.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1245899 HAMILTON-C1 HAMILTON-C1 CBK HAMILTON MEDCIAL AG HAMILTON-C1 07630002800747

Patients

Seq Age Sex Outcome Treatment
1 Unknown Death