Product Wiki · Recalls · U.S. FDA — Device Enforcement

Recall Z-0170-2019 — Mindray BeneVision Distributed Monitoring System (DMS), Part No. 115-034413-00

U.S. FDA — Device Enforcement · United States · 2018-08-30 · Class II

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-0170-2019
Date of alert
2018-08-30
Country / jurisdiction
United States
Risk level
Class II
Risk type
recall
Brand
Mindray DS USA, Inc. dba Mindray North America
Product category
device
Product type
Devices
Reported risk: The firm has identified performance anomalies with the device caused when more than 64 TD60 telemetry transmitters have been connected to a central station. The anomaly causes some ECG waveforms to appear as a flat line at the centralized viewing station and will manifest if more than 64 TD60 transmitters have been connected to a given central station server. Each central station supports only 32 transmitters at a time. For the issue to manifest, the BeneVision DMS needs to be configured to use flexible device assignment, have more than 64 TD60 transmitters, and the workflow must allow 64 TD60s to move around between multiple central stations in the same care area.
Primary source: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts

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