ClearanceBrief
Recall Z-1106-2017 ยท OUG Medical Device Data System

Philips Electronics North America Corporation

Philips Cisco 3850 layer 3 switch, 865339 model WS-C3850-12S-E in use with IntelliVue Information Center iX or Classic Information Center

DateDec 27, 2016
StatusTerminated
ReasonMay experience a loss of centralized monitoring.
Root causeUnder Investigation by firm
ActionPhilips sent an Field Safety Notice on December 27, 2016, to customers via certified mail. The notice explains the issue and informs the customers that no actions are required. The product may be used until the replacement cable is made available. If you need any further information or support concerning this issue, please call your local Philips Representative at (800) 722-9377.
Quantity107
DistributionWorldwide Distribution - US Distribution to the states of : AK CA CO FL GA KY NC NE NH NJ NY OH PA SC TN TX VA WA and WV., and to the countries of : Canada, Germany, Japan, New Zealand, Poland and United Kingdom
FDA recordOpen on fda.gov

510(k) clearances named in this recall

This recall record lists no 510(k) number.