International safety notice

Capio RP Suture Capturing Device

Swiss / SwissMedic · CHE · Feb 21, 2018

Key facts

Title Capio RP Suture Capturing Device
Regulator Swiss / SwissMedic
Country CHE
Brand Capio RP Suture Capturing Device
Manufacturer Boston Scientific Corporation
Models M0068312321, M0068321010, M0068318250, 93420, M0068318261, M0068318150, 00035, M0068318170, M0068311251, 95941, 78960, 53343 and 3 more
Event type Safety Notice
Date Feb 21, 2018
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