Reported Feb 6, 2013 · Terminated

Mindray DPM5 Monitor, a vital signs monitor used on human patients in healthcare facilities.

Mindray DS USA, Inc. d.b.a. 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. d.b.a. Mindray North America · 800 MacArthur Blvd. · Mahwah, NJ · 07430

Is this the product you have?

  • Mindray DPM5 Monitor, a vital signs monitor used on human patients in healthcare facilities.
Lot codes and dates
  • p/n 9201F-PA000XX DS-
    • 0C000565
    • 02000335
    • 12000603
    • 12000599
    • 12000597
    • OCOOO569
    • 9A000247
    • 9A000252
    • 17000648
    • 06000490
    • 05000470
    • 05000466
    • 02000373
Amount recalled
13 units

Where it was sold

Why it was recalled

Mindray has identified an issue with the DPM5 monitors where ST and Arrhythmia features may not be available.

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

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Where this came from

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

Read the FDA (openFDA device enforcement) notice

Notice updated Oct 22, 2013 · Data as of Sep 19, 5:35 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.