Mindray DS USA, Inc. dba Mindray North America: Medical Device Recall in 2014 - (Recall #: Z-0837-2015)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2014.

Data Source: FDA.

Product Description:

DPM 6 Patient Monitor and DPM 7 Patient Monitor. The product affected is the Mindray IBP module, P/N is 6800-30-50485 for use with Mindray DPM 6 and DPM 7 patient monitors . Intended to be used for monitoring, displaying, reviewing, storing and alarming of multiple physiological parameters.

Product Classification:

Class II

Date Initiated: October 6, 2014

Date Posted: December 31, 2014

Recall Number: Z-0837-2015

Event ID: 69788

Reason for Recall:

Mindray has identified an issue that involves the IBP module used with the DPM 6 and DPM 7 Monitor where the IBP measurement data may be displayed in an incorrect IBP tile on the monitors display.

Status: Terminated

Product Quantity: 455 units

Code Information:

DPM 6 - PN: C-047-000199-00 and DPM 7 - PN: C-047-000200-00, IBP Module P/N: 6800-30-50485

Distribution Pattern:

Distributed to the states of AL, CA, CO, FL, GA, IA, IL, IN, LA. MA, MO, MS, MT, NC, ND, NY, OH, PA, SC, TX, VA, WA and WV.

Voluntary or Mandated:

Voluntary: Firm initiated