Product Wiki · Recalls · U.S. FDA — Device Enforcement

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. The device can also set independent alarm limits for data send by the bedside monitor.

U.S. FDA — Device Enforcement · United States · 2014-01-08 · Class II

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-1156-2014
Date of alert
2014-01-08
Country / jurisdiction
United States
Risk level
Class II
Risk type
recall
Brand
Mindray DS USA, Inc. dba Mindray North America
Product category
device
Product type
Devices
Reported risk: 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.
Primary source: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts

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