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Mindray DS USA, Inc. dba Mindray North America recalls Mindray DPM 7 Monitor, Multi Parameter Patient Monitor (with Arrhythmia Detection and Alarms) Intended to be used for
Recalled September 16, 2015 · FDA recall Z-2737-2015 · Mindray DS USA, Inc.
Hazard
The DPM 7 Monitors may display a black screen. · FDA Class II
Units
13 units
Sold at
Distributed to the states of CT, IA, KY, MS, PA, UT and WA.
Description
The DPM 7 Monitors may display a black screen.
Product
Mindray DPM 7 Monitor, Multi Parameter Patient Monitor (with Arrhythmia Detection and Alarms) Intended to be used for monitoring, displaying, reviewing, storing and alarming of multiple physiological parameters including ECG (3-lead or 5-lead selectable), arrhythmia detection, ST Segment analysis, and heart rate.
Manufacturer(s)
Mindray DS USA, Inc. dba Mindray North America
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →