Mindray DS USA, Inc. dba Mindray North America: Medical Device Recall in 2014 - (Recall #: Z-1156-2014)

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:

Panaroma Central Station Product Usage: This device can view real time, store, print, graph, and trend patient clinical and demographic data. The device can also set independent alarm limits for data send by the bedside monitor.

Product Classification:

Class II

Date Initiated: January 8, 2014

Date Posted: March 19, 2014

Recall Number: Z-1156-2014

Event ID: 67495

Reason for Recall:

Mindray has identified two issues with the Panorama Central Station. Full Disclosure data may lag behind the Panorama system time clock when the Panorama Central Station is in use with Mindray¿s V-Series Monitor. Additionally, event indicators lag behind the Panorama system time clock when the Panorama Central Station is in use with a Panorama Telepack.

Status: Terminated

Product Quantity: 732 units in the US

Code Information:

p/n 0998-00-0708-01; 0998-UC-0708-01 and 0020-00-0205-XXX

Distribution Pattern:

Worldwide Distribution - USA Nationwide Distribution

Voluntary or Mandated:

Voluntary: Firm initiated