International safety notice

Urgent Field Safety Notice for Guider Softip XF Guide Catheter by Boston Scientific Corporation Natick

Germany / BfArM · DEU · Feb 17, 2023

Key facts

Title Urgent Field Safety Notice for Guider Softip XF Guide Catheter by Boston Scientific Corporation Natick
Regulator Germany / BfArM
Country DEU
Brand Guider Softip XF Guide Catheter
Manufacturer Boston Scientific Corporation Natick
Models 29308869, 250427, H965100440, 08714729202486
Date Feb 17, 2023
Regulator page bfarm.de

At a glance

  • No Recall
  • No Field safety notice
  • 1–9 Matching device models 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