Remote Network Station RNS-6803-7460Recalls & reported problems
Nihon Kohden Digital Health Solutions, LLC · Remote Network Station with Dell OptiPlex 7460 23.8" All-In-One Computer · Class 2
Data updated Oct 16, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 4
- Deaths reported
- 1
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 4 adverse event reports that list this exact device (DI 00851725007184), received between Feb 23, 2021 and Aug 13, 2025 — classified as 1 death, 3 malfunctions.
The most frequently reported specific device problem is “Protective Measures Problem” (3 reports).
Reports come from manufacturers, hospitals and patients and are not verified by the FDA. A report does not prove the device caused the event, and counts can't be used to compare devices or estimate failure rates. What reports can and can't tell you · How this data works · Data updated Oct 16, 2026.
Reports received per month
Most reported problems
Device problems
- Protective Measures Problem3
- Device Alarm System2
- No Audible Alarm2
- Application Program Problem1
- Audible Prompt/Feedback Problem1
- Communication or Transmission Problem1
Patient problems
- No Clinical Signs, Symptoms or Conditions4
Recent adverse event reports
The 4 most recent of 4 reports, in the reporter's own words as published by the FDA.
MalfunctionAug 13, 2025Device Alarm System; Protective Measures Problem; Device Alarm System; Protective Measures Problem
THE BIOMEDICAL ENGINEER (BME) REPORTED THAT THE REMOTE NETWORK STATION (RNS) DID NOT ALARM FOR A PATIENT'S VENTRICULAR TACHYCARDIA. NO PATIENT HARM WAS REPORTED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 22795597 ↗MalfunctionMar 4, 2023Communication or Transmission Problem; Communication or Transmission Problem
THE CUSTOMER IT/IS CONTACT REPORTED THAT ALL OF THEIR DEVICES ARE INTERMITTENTLY GOING IN AND OUT COMMUNICATION LOSS FOR ROUGHLY 30 SECONDS AT A TIME AND THEN COME BACK UP. THE CENTRAL NURSE'S STATION (CNS) / REMOTE NETWORK STATION (RNS) ARE ALL WIRED. THE BEDSIDE MONITORS ARE USING WIRELESS PACKS. THEY DO NOT KNOW IF ALL OF THE WIRELESS PACKS ARE DISCONNECTING ALL AT ONCE OR IF THE WHOLE NETWORK IS BECAUSE IT SHOWS COMM LOSS ON ALL TILES, SO IT IS HARD TO DETERMINE IF THE CNS IS GOING DOWN OR NOT AS WELL (IF THIS IS HAPPENING ON ONLY WIRELESS DEVICES OR ALL DEVICES). THE CUSTOMER SAID THAT THEY RECENTLY REPLACED ALL THE ACCESS POINTS (APS), AND THEY HAVE BEEN WORKING NORMALLY UNTIL NOW. NIHON KOHDEN COMPUTER INFORMATION TECHNOLOGY SYSTEMS SUPPORT (CITS) REMOTED INTO THE SERVERS. CITS CHECKED THE HOST 1000 SERVER AND NOTICED THAT THE SERVER WAS SET TO BROADCAST MODE, WHICH MEANT NO ISSUES THERE. CITS ALSO CHECKED THE DEVICES AND NOTICED THAT THESE WIRELESS DEVICES WERE NOT UTILIZING THE EG FOR WIRELESS COMMUNICATION. CITS TOOK A PACKET CAPTURE BUT DID NOT SEE ANY RELEVANT EVIDENCE OF LARGE DROPOUTS AND THE SERVERS ARE NOT INVOLVED WITH THIS ISSUE. TECH SUPPORT (TS) AND QA CONTACTED
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 16483285 ↗DeathJul 18, 2022No Audible Alarm; Protective Measures Problem; Audible Prompt/Feedback Problem; No Audible Alarm; Protective Measures Problem; Audible Prompt/Feedback Problem
THE CUSTOMER REPORTED THAT THIS REMOTE NURSE'S STATION (RNS) DID NOT ALARM; HOWEVER, THE CENTRAL NURSE'S STATION (CNS) DID ALARM. THIS CAUSED A DELAY IN TREATMENT AND THE PATIENT PASSED AWAY.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 15048674 ↗MalfunctionFeb 23, 2021Device Alarm System; No Audible Alarm; Application Program Problem; Protective Measures Problem; Device Alarm System; No Audible Alarm; Application Program Problem; Protective Measures Problem
THE BIOMEDICAL ENGINEER (BME) REPORTED THAT THE REMOTE NETWORK SYSTEM (RNS) DID NOT HAVE AN AUDIBLE ALARM FOR THE SPO2 ALARM AND SAID THAT THE PATIENT SPO2 WENT DOWN TO 40. THE RNS WAS SHOWING THE ALARM VISUALLY, BUT IT WAS NOT MAKING AN AUDIBLE SOUND FOR IT. THEY WERE ABLE TO GET THE AUDIBLE ALARM TO WORK AGAIN BY REBOOTING THE RNS. THERE WAS NO PATIENT DEATH, BUT THEY DO NOT KNOW IF THERE WAS INJURY. THE NURSES TOLD HIM THAT THE PATIENT WAS CLOSE TO DEATH. THE BIOMED STATED THAT THE STAFF WAS ABLE TO PROVIDE AID TO THE PATIENT BECAUSE THERE WAS ANOTHER RNS WHICH WAS GIVING AN AUDIBLE ALARM AND THAT WAS HOW THE STAFF WAS ALERTED AND INFORMED. THE BEDSIDE MONITOR ON THE PATIENT WAS GIVING AN AUDIBLE ALARM AS WELL. THIS PATIENT WAS A COVID PATIENT, AND THE DOOR WAS CLOSED FOR THIS ROOM, SO THEY COULD NOT HEAR THE AUDIBLE ALARM COMING IT. NORMALLY FOR NON-COVID PATIENTS, THEY WOULD LEAVE THE DOOR OPEN. ONLY THIS RNS WAS NOT GIVING AN AUDIBLE ALARM. THE RNS IS A SECONDARY MONITORING SYSTEM. THE CENTRAL NURSE'S STATION (CNS) IS THE PRIMARY MONITORING SYSTEM. THIS INCIDENT OCCURRED ON (B)(6) 2021, AT AROUND 2 AM. ON BEDNAME: WHP3510-01. THE BIOMED COULD NOT PROVIDE THE MODEL AND SERIAL
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 11369863 ↗
Other MONITOR, PHYSIOLOGICAL, PATIENT(WITH ARRHYTHMIA DETECTION OR ALARMS) devices
- IntelliVue MX40 1.4GHz MX40 1.4 GHz Smart HoppingPhilips Medical Systems Hsg · MONITOR, PHYSIOLOGICAL, PATIENT(WITH ARRHYTHMIA DETECTION OR ALARMS)1 recall47 deaths2,541 reports
- NA PU-621RNihon Kohden Corporation · MONITOR, PHYSIOLOGICAL, PATIENT(WITH ARRHYTHMIA DETECTION OR ALARMS)17 deaths1,666 reports
- Tempus Pro 00-1024-RRemote Diagnostic Technologies Limited · Monitor, Physiological, Patient(With Arrhythmia Detection Or Alarms)7 recalls8 deaths1,217 reports
- NA PU-681RANihon Kohden Corporation · MONITOR, PHYSIOLOGICAL, PATIENT(WITH ARRHYTHMIA DETECTION OR ALARMS)22 deaths1,493 reports
- IntelliVue Multi-Measurement Module X3 IntelliVue X3Philips Medizin Systeme Böblingen GmbH · MONITOR, PHYSIOLOGICAL, PATIENT(WITH ARRHYTHMIA DETECTION OR ALARMS)1 recall19 deaths1,172 reports
- Patient Information Center IXPhilips Medical Systems Hsg · MONITOR, PHYSIOLOGICAL, PATIENT(WITH ARRHYTHMIA DETECTION OR ALARMS)82 deaths941 reports
- Patient Information Center iXPhilips Medical Systems Hsg · MONITOR, PHYSIOLOGICAL, PATIENT(WITH ARRHYTHMIA DETECTION OR ALARMS)83 deaths814 reports
- Tempus Pro 00-1024-RRemote Diagnostic Technologies Limited · Monitor, Physiological, Patient(With Arrhythmia Detection Or Alarms)5 recalls541 reports
Sources and updates
- Device record: FDA GUDID, file dated Oct 13, 2026 · View this device in AccessGUDID ↗
- Adverse event reports: FDA MAUDE, file dated Oct 14, 2026 · each report above links to its original FDA record
- Recalls: FDA Medical Device Recalls, file dated Oct 16, 2026
- Page last rebuilt: Oct 16, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
How reports and recalls are matched · Editorial policy · Report an error on this page