Mindray DS USA, Inc. d.b.a. Mindray North America: Medical Device Recall in 2013 - (Recall #: Z-0742-2013)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2013.

Data Source: FDA.

Product Description:

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

Product Classification:

Class II

Date Initiated: September 5, 2012

Date Posted: February 6, 2013

Recall Number: Z-0742-2013

Event ID: 63800

Reason for Recall:

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

Status: Terminated

Product Quantity: 13 units

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

Voluntary or Mandated:

Voluntary: Firm initiated