FDA Adverse Event Malfunction Summary report: N

CNS-6801A

MDR report key: 9300128 · Received November 8, 2019

Report

Report Number
8030229-2019-00642
Event Type
Malfunction
Date Received
November 8, 2019
Date of Event
October 17, 2019
Report Date
February 13, 2020
Manufacturer
NIHON KOHDEN CORPORATION
Product Code
MHX
UDI-DI
04931921131640
PMA / PMN Number
K102376
Removal / Correction Number
NA
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
MI, US
Reporter Occupation
BIOMEDICAL ENGINEER

Narratives

Additional Manufacturer Narrative · 0

DETAILS OF THE COMPLAINT: CUSTOMER AT MERCY HEALTH PARTNERS REPORTED THE FOLLOWING ISSUE: 10/17 @1125 COMM LOSS 6 SECONDS THIS WAS PROVIDED TO NKA TECHNICAL SUPPORT (TS) FROM THE HOSPITAL'S DEPARTMENT LOGS. NO FURTHER INFORMATION WILL BE PROVIDED FROM THE HOSPITAL. INVESTIGATION CONCLUSION: THERE WAS A DOCUMENTED INCIDENT IN WHICH THE CNS WAS REPORTED TO HAVE COMMUNICATION LOSS. THE DETAILS SURROUNDING THE INCIDENT WERE NOT PROVIDED AND INFORMATION ON THE EXTENT OF ANY TROUBLESHOOTING IS UNKNOWN. FURTHER INVESTIGATION OF THE ISSUE IS LIMITED AS THE DEVICE AND/OR LOGS WERE NOT RETRIEVED FOR EVALUATION, NOR WAS THE DEVICE SERIAL NUMBER PROVIDED. THE CUSTOMER WAS NOT WILLING TO PROVIDE FURTHER INFORMATION. THIS WAS CONFIRMED UNDER NOTIFICATION 300182278 (TICKET (B)(4)). BASED ON THE INFORMATION PROVIDED, NO ROOT CAUSE ANALYSIS OR RISK ASSESSMENT COULD BE PERFORMED. ADDITIONAL DEVICE INFORMATION: D11 & C2 CONCOMITANT MEDICAL DEVICE INFORMATION: THE CUSTOMER STATED THAT THE CNS WAS MONITORING GZ TELEMETRY TRANSMITTERS, BUT NO MODEL OR SERIAL NUMBERS WERE PROVIDED.

Description of Event or Problem · 0

THE BIOMEDICAL ENGINEER REPORTED THAT ON LOG 6, 6TH FLOOR (B)(6) 2019 AT 1125 COMM LOSS 6 SECONDS. THE CUSTOMER STATED THAT ALL COMMUNICATION LOSS ISSUES ARE ON THE CENTRAL NURSE'S STATION (CNS) AND MONITORING GZ TELEMETRY TRANSMITTERS. THIS TICKET HAS BEEN CREATED TO DOCUMENT THE DEPARTMENT LOGS FROM THE HOSPITAL. THE HOSPITAL WILL NOT BE PROVIDING ANY ADDITIONAL INFORMATION. NO PATIENT HARM WAS REPORTED.

Additional Manufacturer Narrative · 1

THE BIOMEDICAL ENGINEER REPORTED THAT ON LOG 6, 6TH FLOOR 10/17/19 AT 1125 COMM LOSS 6 SECONDS. THE CUSTOMER STATED THAT ALL COMMUNICATION LOSS ISSUES ARE ON THE CENTRAL NURSE'S STATION (CNS) AND MONITORING GZ TELEMETRY TRANSMITTERS. THIS TICKET HAS BEEN CREATED TO DOCUMENT THE DEPARTMENT LOGS FROM THE HOSPITAL. THE HOSPITAL WILL NOT BE PROVIDING ANY ADDITIONAL INFORMATION. NO PATIENT HARM WAS REPORTED. NIHON KOHDEN CONTINUES TO INVESTIGATE THE REPORTED EVENT. NIHON KOHDEN WILL SUBMIT A SUPPLEMENTAL REPORT IN ACCORDANCE WITH 21 CFR SECTION 803.56 WHEN ADDITIONAL INFORMATION BECOMES AVAILABLE. CONCOMITANT MEDICAL DEVICE INFORMATION: THE CUSTOMER STATED THAT THE CNS WAS MONITORING GZ TELEMETRY TRANSMITTERS, BUT NO MODEL OR SERIAL NUMBERS WERE PROVIDED.

Description of Event or Problem · 1

THE BIOMEDICAL ENGINEER REPORTED THAT ON LOG 6, 6TH FLOOR (B)(6) 2019 AT 1125 COMM LOSS 6 SECONDS. THE CUSTOMER STATED THAT ALL COMMUNICATION LOSS ISSUES ARE ON THE CENTRAL NURSE'S STATION (CNS) AND MONITORING GZ TELEMETRY TRANSMITTERS. THIS TICKET HAS BEEN CREATED TO DOCUMENT THE DEPARTMENT LOGS FROM THE HOSPITAL. THE HOSPITAL WILL NOT BE PROVIDING ANY ADDITIONAL INFORMATION. NO PATIENT HARM WAS REPORTED.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1094335 CNS-6801A CENTRAL MONITOR SYSTEM MHX NIHON KOHDEN CORPORATION CNS-6801A NA 04931921131640

Patients

Seq Age Sex Outcome Treatment
1 GZ TRANSMITTERS| GZ TRANSMITTERS