FDA Adverse Event Malfunction Summary report: N

CNS-6801A

MDR report key: 12340293 · Received August 18, 2021

Report

Report Number
2080783-2021-01495
Event Type
Malfunction
Date Received
August 18, 2021
Date of Event
July 21, 2021
Report Date
August 18, 2021
Manufacturer
NIHON KOHDEN CORPORATION
Product Code
MHX
UDI-DI
04931921131640
Product Problem
Yes
Report Source
Distributor report
Reporter Location
TN, US
Reporter Occupation
BIOMEDICAL ENGINEER

Narratives

Additional Manufacturer Narrative · 1

THE CUSTOMER REPORTED THAT THE CENTRAL NURSE'S STATION (CNS) SHOWS A BEDSIDE MONITOR IN COMMUNICATION LOSS. THE CUSTOMER LATER REPORTED THAT THE COMMUNICATION LOSS ISSUE HAD BEEN RESOLVED WITH NOT OTHER INFORMATION. THERE WAS NO PATIENT INJURY 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. ATTEMPT # 1: ON 08/02/2021 EMAILED THE CUSTOMER VIA MICROSOFT OUTLOOK FOR PATIENT INFORMATION: NO REPLY WAS RECEIVED. ATTEMPT # 2: ON 08/09/2021 EMAILED THE CUSTOMER VIA MICROSOFT OUTLOOK FOR PATIENT INFORMATION: THE CUSTOMER REPLIED BY STATING; I'M NOT FAMILIAR WITH THIS TICKET. ATTEMPT # 1: ON 08/02/2021 EMAILED THE CUSTOMER VIA MICROSOFT OUTLOOK FOR PATIENT INFORMATION: NO REPLY WAS RECEIVED. ATTEMPT # 2: ON 08/09/2021 EMAILED THE CUSTOMER VIA MICROSOFT OUTLOOK FOR PATIENT INFORMATION: THE CUSTOMER REPLIED BY STATING; I'M NOT FAMILIAR WITH THIS TICKET. ATTEMPT # 1: ON 08/02/2021 EMAILED THE CUSTOMER VIA MICROSOFT OUTLOOK FOR PATIENT INFORMATION: NO REPLY WAS RECEIVED. ATTEMPT # 2: ON 08/09/2021 EMAILED THE CUSTOMER VIA MICROSOFT OUTLOOK FOR PATIENT INFORMATION: THE CUSTOMER REPLIED BY STATING; I'M NOT FAMILIAR WITH THIS TICKET. ADDITIONAL MODEL INFORMATION: CONCOMITANT MEDICAL DEVICE: THE FOLLOWING DEVICE WAS USED IN CONJUNCTION WITH THE CENTRAL NURSE'S STATION (CNS): BEDSIDE MONITOR (BSM): MODEL #: NI; SERIAL #: NI; DEVICE MANUFACTURER DATA: NI; UNIQUE IDENTIFIER (UDI) #: NI; RETURNED TO NIHON KOHDEN: NI.

Description of Event or Problem · 1

THE CUSTOMER REPORTED THAT THE CENTRAL NURSE'S STATION (CNS) SHOWS A BEDSIDE MONITOR IN COMMUNICATION LOSS. THERE WAS NO PATIENT INJURY REPORTED.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1232392 CNS-6801A CENTRAL MONITOR SYSTEM MHX NIHON KOHDEN CORPORATION CNS-6801A NA 04931921131640

Patients

Seq Age Sex Outcome Treatment
1 BSM