International safety notice

Proteus XR/a

Swiss / SwissMedic · CHE · Jul 14, 2014

Key facts

Title Proteus XR/a
Regulator Swiss / SwissMedic
Country CHE
Brand Proteus XR/a
Manufacturer GE Healthcare
Models 800014110, 22973, 2357602-100, 53226, 7979293186, Rév.30, Rév.10, 800917294, 800917293, 2261765, 2-5-2, 2273022-100 and 12 more
Event type Safety Notice
Date Jul 14, 2014
Regulator page fsca.swissmedic.ch

At a glance

  • No Recall
  • Yes Field safety notice
  • 1–9 Matching device models in FDA data
  • 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