International safety notice

Catéter de angiografía IMAGER™ II de 5F. Ver referencias afectadas del envase exterior e interior en la nota de aviso de la empresa.

Spain / AEMPS · ESP · Feb 19, 2020

Key facts

Title Catéter de angiografía IMAGER™ II de 5F. Ver referencias afectadas del envase exterior e interior en la nota de aviso de la empresa.
Regulator Spain / AEMPS
Country ESP
Brand Catéter de angiografía IMAGER™ II de 5F. Ver referencias afectadas del envase exterior e interior en la nota de aviso de la empresa.
Manufacturer Boston Scientific Corporation, Estados Unidos.
Models 12-MAR-2021, M001314340, 8-JUN-2020, 08714729354963, 16-JUL-2020, M001314590, 08714729355892, M001314140, 13-JUL-2020, 10-AUG-2020, 134631, 08714729354888 and 49 more
Event type Safety Notice
Date Feb 19, 2020

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