BeneVision Central Monitoring SystemRecalls & reported problems across all models
Shenzhen Mindray Bio-Medical Electronics Co., Ltd. · 2 models in the FDA device registry
Data updated Oct 18, 2026 from official FDA records · Editorial policy
1 open recall names at least one BeneVision Central Monitoring System model. Check whether yours is affected in the recall details, and contact the manufacturer or your healthcare provider.
- Adverse event reports
- 7
- Deaths reported
- 2
- Injuries reported
- 0
- Recalls
- 1
We found 2 models of BeneVision Central Monitoring System by Shenzhen Mindray Bio-Medical Electronics Co., Ltd. in the FDA's device registry (GUDID). Together they are named in 7 adverse event reports in the FDA's MAUDE database, received between Feb 11, 2021 and Feb 25, 2026 — classified as 2 deaths, 5 malfunctions.
The most frequently reported specific device problem is “Device Alarm System” (5 reports).
1 FDA recall record name at least one of these models by its device identifier, 1 still open.
Reports come from manufacturers, hospitals and patients and are not verified by the FDA. A report does not prove the device caused the event. Widely used products collect more reports, so totals can't be used to compare products or estimate failure rates. Only reports that name a model's exact device identifier are counted. What reports can and can't tell you · How this data works
Reports received per month, all models
BeneVision Central Monitoring System recalls
FDA recall records that name at least one of these models by its device identifier, newest first. Each recall usually covers specific models or lots, so check the details.
- Nov 18, 2025Class IIOpen, Classified
When the Worstation of the BeneVision DMS has a specific hardware configuration, the computer may experience audio playback failure or screen freezing.
Z-0920-2026 · Root cause: Software design · Recall details · FDA record ↗
Most reported BeneVision Central Monitoring System problems
Device problems
- Device Alarm System5
- No Audible Alarm5
Patient problems
- No Clinical Signs, Symptoms or Conditions4
- Insufficient Information3
- Arrhythmia2
BeneVision Central Monitoring System models
2 models, most reported first. Each model has its own page with its reports, recalls and device details.
- BeneVision Central Monitoring SystemSystem, Network And Communication, Physiological Monitors1 recall2 deaths5 reports
- BeneVision Central Monitoring SystemSystem,Network And Communication,Physiological Monitors2 reports
Recent BeneVision Central Monitoring System adverse event reports
The 7 most recent reports across all models, in the reporter's own words as published by the FDA.
DeathFeb 25, 2026Device Alarm System
NO DEVICE MALFUNCTION WAS REPORTED BY THE CUSTOMER. IT WAS REPORTED THAT BETWEEN (B)(6) 2026, AT APPROXIMATELY 23:30 AND (B)(6) 2026, AT APPROXIMATELY 01:00, A PATIENT CONNECTED TO A TM80 UNIT AND SUBSEQUENTLY CONNECTED TO A BENEVISION DISTRIBUTED MONITORING SYSTEM (DMS) WORKSTATION EXPIRED WHILE NOT CONNECTED TO ECG LEADS. DURING THIS TIME PERIOD, THE PATIENT HAD REMOVED THE ECG LEADS. AS A RESULT, A "PATIENT DISCONNECTED FROM ECG" ALARM WAS PRESENT, AND NO CARDIAC RHYTHM ALARMS WERE GENERATED. CLINICAL STAFF WERE UNABLE TO ACKNOWLEDGE/SILENCE ALARMS FROM WORKSTATION DUE TO PRIOR EVENT.
Patient problems: Arrhythmia
MAUDE report 24446328 ↗DeathFeb 25, 2026Device Alarm System
NO DEVICE MALFUNCTION WAS REPORTED BY THE CUSTOMER. IT WAS REPORTED THAT BETWEEN (B)(6) 2026, AT APPROXIMATELY 23:30 AND (B)(6) 2026, AT APPROXIMATELY 01:00, A PATIENT CONNECTED TO A TM80 UNIT AND SUBSEQUENTLY CONNECTED TO A BENEVISION DISTRIBUTED MONITORING SYSTEM (DMS) WORKSTATION EXPIRED WHILE NOT CONNECTED TO ECG LEADS. DURING THIS TIME PERIOD, THE PATIENT HAD REMOVED THE ECG LEADS. AS A RESULT, A "PATIENT DISCONNECTED FROM ECG" ALARM WAS PRESENT, AND NO CARDIAC RHYTHM ALARMS WERE GENERATED. CLINICAL STAFF WERE UNABLE TO ACKNOWLEDGE/SILENCE ALARMS FROM WORKSTATION DUE TO PRIOR EVENT.
Patient problems: Arrhythmia
MAUDE report 24446326 ↗MalfunctionJun 12, 2025Device Alarm System; No Audible Alarm; Device Alarm System; No Audible Alarm
IT WAS REPORTED THAT ON (B)(6) 2025, A VENTRICULAR TACHYCARDIA (V-TACH) ALARM WAS MISSED; THE SYSTEM DID NOT GENERATE AN ALARM FOR V-TACH. NO PATIENT INJURY WAS REPORTED.
Patient problems: Insufficient Information
MAUDE report 22197277 ↗MalfunctionJun 12, 2025Device Alarm System; No Audible Alarm; Device Alarm System; No Audible Alarm
IT WAS REPORTED THAT ON (B)(6) 2025, AT 8:35AM, THE PATIENT ON A TM80 TELEMETRY UNIT (TELE ID 55) WAS IN VENTRICULAR TACHYCARDIA (V-TACH) FOR 5 BEATS AND THE SYSTEM DID NOT GENERATE A V-TACH ALARM. NO PATIENT INJURY WAS REPORTED.
Patient problems: Insufficient Information; No Clinical Signs, Symptoms or Conditions
MAUDE report 22197272 ↗MalfunctionJun 12, 2025Device Alarm System; No Audible Alarm; Device Alarm System; No Audible Alarm
IT WAS REPORTED THAT ON (B)(6) 2025, AT 8:35AM, THE PATIENT ON A TM80 TELEMETRY UNIT (TELE ID 55) WAS IN VENTRICULAR TACHYCARDIA (V-TACH) FOR 5 BEATS AND THE SYSTEM DID NOT GENERATE A V-TACH ALARM. NO PATIENT INJURY WAS REPORTED.
Patient problems: Insufficient Information; No Clinical Signs, Symptoms or Conditions
MAUDE report 22197267 ↗MalfunctionFeb 12, 2021No Audible Alarm; No Audible Alarm
THE CUSTOMER REPORTED THAT AROUND 8:14AM ON (B)(6) 2021 A PATIENT WAS IN BRADYCARDIA AND NO AUDIBLE ALARM WAS HEARD AT THE BENEVISION DMS. A VISUAL ALARM WAS NOTED. NO PATIENT INJURY WAS REPORTED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 11321147 ↗MalfunctionFeb 11, 2021No Audible Alarm; No Audible Alarm
THE CUSTOMER REPORTED THAT AROUND 8:14AM ON (B)(6) 2021 A PATIENT WAS IN BRADYCARDIA AND NO AUDIBLE ALARM WAS HEARD AT THE BENEVISION DMS. A VISUAL ALARM WAS NOTED. NO PATIENT INJURY WAS REPORTED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 11318691 ↗
Sources and updates
- Models: FDA GUDID, file dated Oct 13, 2026. Models are grouped by the brand name the manufacturer registered.
- Adverse event reports: FDA MAUDE, file dated Oct 14, 2026
- Recalls: FDA Medical Device Recalls, file dated Oct 16, 2026
- Page last rebuilt: Oct 18, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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