FDA Device recall Z-1156-2014

Panaroma Central Station Product Usage: This device can view real time, store, print, graph, and trend patient clinical and demographic data

• FDA Device
• Class II
• terminated
• Published 2014-03-19

On 2014-03-19 the FDA classified a Class II recall of Panaroma Central Station Product Usage: This device can view real time, store, print, graph, and trend patient clinical and demographic data by Mindray Ds Usa, citing 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….

Read the official FDA Device notice

Product

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.

Reason

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.

Identifiers

Status history

No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:53 UTC. Current status: terminated.

Source

Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1156-2014%22

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