• Decrease font size
  • Return font size to normal
  • Increase font size
U.S. Department of Health and Human Services

Enforcement Report - Week of February 6, 2013

  • Print
  • Share
  • E-mail

Product Detail

Product Description Mindray, DPM5 Monitor, a vital signs monitor used on human patients in healthcare facilities.
Recall Number Z-0742-2013
Classification Class II
Code Info p/n 9201F-PA000XX DS- 0C000565 02000335 12000603 12000599 12000597 0C000569 9A000247 9A000252 17000648 06000490 05000470 05000466 02000373
Product Distributed Qty 13 units
Reason For Recall Mindray has identified an issue with the DPM5 monitors where ST and Arrhythmia features may not be available.

Event Detail

Event Id 63800
Product Type Devices
Status Ongoing
Recalling Firm Mindray DS USA, Inc. d.b.a. Mindray North America
City Mahwah
State NJ
Country US
Voluntary / Mandated Voluntary: Firm Initiated
Recall Initiation Date 2012-09-05
Initial Firm Notification of Consignee or Public Letter
Distribution Pattern US Nationwide Distribution including the states of: VA, TN, FL, & TX