International safety notice

Oxylog VE300

Swiss / SwissMedic · CHE · Apr 16, 2019

Key facts

Title Oxylog VE300
Regulator Swiss / SwissMedic
Country CHE
Brand Oxylog VE300
Manufacturer Drägerwerk AG & Co.KGaA
Models Page2, 882-0, VE300, 23542, 53-55, 23558, Maf1nahme, DE135082211, NOLADE21SPL, 882-2080, 5790200
Event type Safety Notice
Date Apr 16, 2019
Regulator page fsca.swissmedic.ch

At a glance

  • No Recall
  • Yes Field safety notice
  • 1–9 Matching catalog numbers in FDA data

Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.

About International device safety notices

Field safety notices, recalls and safety alerts published by about 30 national medical device regulators outside the United States, matched by Orca1 to FDA device data.

Source: National medical device regulators (as listed), compiled by Orca1

Browse all International device safety notices