FDA Adverse Event Malfunction Summary report: N

HAMILTON-C1

MDR report key: 19040972 · Received April 4, 2024

Report

Report Number
3001421318-2024-00837
Event Type
Malfunction
Date Received
April 4, 2024
Date of Event
February 24, 2024
Report Date
November 7, 2024
Manufacturer
HAMILTON MEDICAL AG
Product Code
CBK
UDI-DI
07630002800747
PMA / PMN Number
K181216
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
IN
Reporter Occupation
OTHER
Health Professional
N

Narratives

Additional Manufacturer Narrative · 0

HAMILTON MEDICAL AG CASE NUMBER IS: (B)(4).

Additional Manufacturer Narrative · 0

HAMILTON MEDICAL AG CASE NUMBER IS: (B)(4).

Description of Event or Problem · 0

THE FOLLOWING WAS REPORTED TO HAMILTON MEDICAL AG: VENTILATOR NOT WORKING (TF: 232029 , 232008) - 'TE232029 TINSTSENSORDEFECT', 'TE232008 PAMBIENTSENSORDEFECT' NO HEALTH CONSEQUENCES OR IMPACT. PATIENT INVOLVEMENT UNKNOWN.

Description of Event or Problem · 0

THE FOLLOWING WAS REPORTED TO HAMILTON MEDICAL AG: VENTILATOR NOT WORKING (TF: 232029 , 232008) - 'TE232029 TINSTSENSORDEFECT', 'TE232008 PAMBIENTSENSORDEFECT'. NO HEALTH CONSEQUENCES OR IMPACT. PATIENT INVOLVEMENT UNKNOWN.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
2335087 HAMILTON-C1 HAMILTON-C1 CBK HAMILTON MEDICAL AG 161001 07630002800747

Patients

Seq Age Sex Outcome Treatment
1 NA Unknown