FDA Adverse Event Malfunction Summary report: N

HAMILTON-C6

MDR report key: 19131638 · Received April 18, 2024

Report

Report Number
3001421318-2024-00941
Event Type
Malfunction
Date Received
April 18, 2024
Date of Event
February 29, 2024
Report Date
October 2, 2024
Manufacturer
HAMILTON MEDICAL AG
Product Code
CBK
UDI-DI
07630002808590
PMA / PMN Number
K201658
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
AS
Reporter Occupation
OTHER HEALTH CARE PROFESSIONAL
Health Professional
Yes

Narratives

Additional Manufacturer Narrative · 0

HAMILTON MEDICAL AG COMES TO THE CONCLUSION: ROOT CAUSE: BLACK OUT DURING HMI CONTROLLER RESET. CORRECTION: INSTALL LATEST SW VERSION. HAMILTON MEDICAL AG COMPLAINT NUMBER: (B)(4). FOLLOW-UP 1 - CORRECTED INFORMATION: **UDI RELATED DATA QUALITY UPDATES ONLY** FIELD D4 WAS UPDATED WITH FULL UDI INFORMATION.

Additional Manufacturer Narrative · 0

HAMILTON MEDICAL AG COMES TO THE CONCLUSION: ROOT CAUSE: BLACK OUT DURING HMI CONTROLLER RESET. CORRECTION: INSTALL LATEST SW VERSION.

Description of Event or Problem · 0

THE FOLLOWING WAS REPORTED TO HAMILTON MEDICAL AG: SUMMARY: INTERACTION PANEL BLACKOUT FOR 2-3 SEC (HMI RESET).

Description of Event or Problem · 0

THE FOLLOWING WAS REPORTED TO HAMILTON MEDICAL AG: SUMMARY: INTERACTION PANEL BLACKOUT FOR 2-3 SEC (HMI RESET).

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
456069 HAMILTON-C6 HAMILTON-C6 VENTILATOR CBK HAMILTON MEDICAL AG 160021 07630002808590

Patients

Seq Age Sex Outcome Treatment
1 NA Unknown