International safety notice

Allura Xper

Swiss / SwissMedic · CHE · Mar 9, 2015

Key facts

Title Allura Xper
Regulator Swiss / SwissMedic
Country CHE
Brand Allura Xper
Manufacturer Philips Medical Systems BV
Models 7.2.xCodes, R7.2.8, 722020, FCO72200270, R7.2.xCodici, 1003.2, 722005, 21CFR1020.32, 722006, XCR603-150018, R7.2.x, 722008 and 11 more
Event type Safety Notice
Date Mar 9, 2015
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