FDA Adverse Event Malfunction Summary report: N

HAMILTON MEDICAL AG

MDR report key: 16766394 · Received April 18, 2023

Report

Report Number
3001421318-2023-01485
Event Type
Malfunction
Date Received
April 18, 2023
Date of Event
April 13, 2023
Report Date
August 24, 2023
Manufacturer
HAMILTON MEDICAL AG
Product Code
CBK
UDI-DI
07630002808590
PMA / PMN Number
K201658
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
NL
Reporter Occupation
OTHER HEALTH CARE PROFESSIONAL
Health Professional
Yes

Narratives

Additional Manufacturer Narrative · 0

HAMILTON MEDICAL AG`S CONCLUSION FOR THIS EVENT: INVESTIGATION ONGOING.

Additional Manufacturer Narrative · 0

HAMILTON MEDICAL AG`S CONCLUSION FOR THIS EVENT: ROOTCAUSE: DEFECTIVE MAINBOARD. CORRECTION: REPLACEMENT OF THE DEFECTIVE COMPONENT.

Description of Event or Problem · 0

THE FOLLOWING WAS REPORTED TO THE HAMILTON MEDICAL AG: DETAILED COMPLAINT AND FAILURE DESCRIPTION: DURING STARTING UP, ACOUSTIC ALARM SOUNDS FOR NO REASON. AFTER SHUTTING DOWN COMPLETELY THE ALARM DISAPPEARED. THE C6 STARTS UP NORMAL AFTERWARDS.

Description of Event or Problem · 0

THE FOLLOWING WAS REPORTED TO THE HAMILTON MEDICAL AG: DETAILED COMPLAINT AND FAILURE DESCRIPTION: DURING STARTING UP, ACOUSTIC ALARM SOUNDS FOR NO REASON. AFTER SHUTTING DOWN COMPLETELY THE ALARM DISAPPEARED. THE C6 STARTS UP NORMAL AFTERWARDS.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1601006 HAMILTON MEDICAL AG HAMILTON-C6 VENTILATOR CBK HAMILTON MEDICAL AG 160001 07630002808590

Patients

Seq Age Sex Outcome Treatment
1 Unknown