FDA Adverse Event Injury Summary report: N

HAMILTON-C3

MDR report key: 19356758 · Received May 21, 2024

Report

Report Number
3001421318-2024-01226
Event Type
Injury
Date Received
May 21, 2024
Date of Event
May 13, 2024
Report Date
November 14, 2024
Manufacturer
HAMILTON MEDICAL AG
Product Code
CBK
UDI-DI
07630002801881
PMA / PMN Number
K201306
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
PL
Reporter Occupation
OTHER HEALTH CARE PROFESSIONAL
Health Professional
Yes

Narratives

Additional Manufacturer Narrative · 0

HAMILTON MEDICAL AG COMES TO THE CONCLUSION: INVESTIGATION ONGOING. 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.

Additional Manufacturer Narrative · 0

HAMILTON MEDICAL AG COMES TO THE CONCLUSION: INVESTIGATION ONGOING.

Description of Event or Problem · 0

THE FOLLOWING WAS REPORTED TO HAMILTON MEDICAL AG: SUMMARY:DEVICE ENTERS AMBIENT MODE AND ALARMS WITH TEQR_BMMONITORING LOGGED IN ERRORLOG.

Description of Event or Problem · 0

THE FOLLOWING WAS REPORTED TO HAMILTON MEDICAL AG: SUMMARY:DEVICE ENTERS AMBIENT MODE AND ALARMS WITH TEQR_BMMONITORING LOGGED IN ERRORLOG.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
583623 HAMILTON-C3 HAMILTON-C3 CBK HAMILTON MEDICAL AG 160005 07630002801881

Patients

Seq Age Sex Outcome Treatment
1 NA Unknown