Mindray DS USA, Inc. dba Mindray North America: Medical Device Recall in 2016 - (Recall #: Z-0701-2016)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2016.

Data Source: FDA.

Product Description:

Panorama Patient Monitoring Network. Software Kit 0020-00-0205-19A, View Station Software Kit 0020-00-0206-16A, Work Station Software Kit 0020-00-0207-16A, Software Kit Upgrade TECH-00-910. The Panaroma Patient Monitoring Network is intended for use in a fixed location in the healthcare facility setting as a central viewing station. It is not intended to be directly connected to patient at any time or installed in a patient's vicinity.

Product Classification:

Class II

Date Initiated: December 15, 2015

Date Posted: February 10, 2016

Recall Number: Z-0701-2016

Event ID: 72864

Reason for Recall:

An issue with the Panorama Central Station may cause the system to spontaneously restart. This may occur after about 49 days of continuous operation. On restart, monitoring will be lost for about 2.5 minutes. Settings and configurations are maintained.

Status: Terminated

Product Quantity: 63 products

Code Information:

version 11.5.1

Distribution Pattern:

Nationwide Distribution.

Voluntary or Mandated:

Voluntary: Firm initiated