Reported Sep 16, 2015 · Terminated

Mindray DPM 7 Monitor, Multi Parameter Patient Monitor (with Arrhythmia Detection and Alarms) Intended to be used for…

Mindray DS USA, Inc. dba Mindray North America

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

What you should do

Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.

Firm contact: Mindray DS USA, Inc. dba Mindray North America · 800 Macarthur Blvd · Mahwah, NJ · 07430-2001

Is this the product you have?

  • 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.
Lot codes and dates
  • Lot #14A18
  • PN6800F-PA00001
  • Serial Numbers
    • DU- 46002583
    • DU-46002587
    • DU-46002588
    • DU-46002589
    • DU-46002592
    • DU-46002594
    • DU-46002595
    • DU-46002596
    • DU-46002599
    • DU-46002600
    • DU-46002601
    • DU-46002605 and DU-46002606
Amount recalled
13 units

Where it was sold

Why it was recalled

The DPM 7 Monitors may display a black screen.

This product could cause temporary or reversible health problems — stop using it.

Want the full recall guide?

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Where this came from

Source: U.S. Food & Drug Administration (openFDA)

Read the FDA (openFDA device enforcement) notice

Notice updated May 2, 2017 · Data as of Sep 19, 4:51 PM UTC

RecallNow is not a government agency. Every fact on this page is published by the FDA, USDA or CPSC and links back to their notice.