Skip to content
Recall Observatory FDA recall evidence

Device product

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

Z-0742-2013

September 05, 2012

Class II

Product summary

Firm
Mindray DS USA, Inc. d.b.a. Mindray North America
Event
Event 63800
Status
Terminated
Classification
Class II
Quantity
13 units
Official record key
device-enforcement:Z-0742-2013

Official wording

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

Code information: p/n 9201F-PA000XX DS- 0C000565 02000335 12000603 12000599 12000597 OCOOO569 9A000247 9A000252 17000648 06000490 05000470 05000466 02000373

Distribution pattern: US Nationwide Distribution including the states of: VA, TN, FL, & TX

Derived failure modes

  • Unknown

    reason.no_named_rule · v1.0.0

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