FDA Adverse Event Malfunction Summary report: N

HAMILTON-C3

MDR report key: 19085836 · Received April 11, 2024

Report

Report Number
3001421318-2024-00897
Event Type
Malfunction
Date Received
April 11, 2024
Date of Event
February 9, 2024
Report Date
November 5, 2024
Manufacturer
HAMILTON MEDICAL AG
Product Code
CBK
UDI-DI
07630002801881
PMA / PMN Number
K201306
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
IN
Reporter Occupation
OTHER HEALTH CARE PROFESSIONAL
Health Professional
Yes

Narratives

Additional Manufacturer Narrative · 0

HAMILTON MEDICAL AG COMES TO THE CONCLUSION: ROOT CAUSE: MAIN BOARD DEFECTIVE. CORRECTION: MAIN BOARD REPLACED.

Additional Manufacturer Narrative · 0

HAMILTON MEDICAL AG COMES TO THE CONCLUSION: ROOT CAUSE: MAINBOARD DEFECTIVE. CORRECTION: MAINBOARD REPLACED. 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, UPDATED FIELDS: B4, D1, D2A, D4, D8, G1, G2, G6, H2, H4, H5.

Description of Event or Problem · 0

THE FOLLOWING WAS REPORTED TO HAMILTON MEDICAL AG: SUMMARY: TF 431008, 231012, 231023 DURING START-UP.

Description of Event or Problem · 0

THE FOLLOWING WAS REPORTED TO HAMILTON MEDICAL AG: SUMMARY: TF 431008, 231012, 231023 DURING START-UP.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1126013 HAMILTON-C3 HAMILTON-C3 CBK HAMILTON MEDICAL AG 160005 07630002801881

Patients

Seq Age Sex Outcome Treatment
1 NA Unknown