FDA Adverse Event Malfunction Summary report: N

HAMILTON-C6

MDR report key: 19295981 · Received May 12, 2024

Report

Report Number
3001421318-2024-01140
Event Type
Malfunction
Date Received
May 12, 2024
Date of Event
January 12, 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
JA
Reporter Occupation
OTHER HEALTH CARE PROFESSIONAL
Health Professional
Yes

Narratives

Additional Manufacturer Narrative · 0

HAMILTON MEDICAL AG COMES TO THE CONCLUSION: ROOT CAUSE: BLOWER DEFECTIVE. CORRECTION: REPLACED DEFECTIVE COMPONENT. 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: BLOWER DEFECTIVE. CORRECTION: REPLACED DEFECTIVE COMPONENT.

Description of Event or Problem · 0

THE FOLLOWING WAS REPORTED TO HAMILTON MEDICAL AG: SUMMARY: TF 232006 (BLOWER TEMPERATURE SENSOR DEFECT) DURING START-UP.

Description of Event or Problem · 0

THE FOLLOWING WAS REPORTED TO HAMILTON MEDICAL AG: SUMMARY: TF 232006 (BLOWERTEMPERATURESENSORDEFECT) DURING START-UP.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
842082 HAMILTON-C6 HAMILTON-C6 VENTILATOR CBK HAMILTON MEDICAL AG 160021 07630002808590

Patients

Seq Age Sex Outcome Treatment
1 NA Unknown