International safety notice

Urgent Field Safety Notice for Oceane+ Hüftschäfte (Standard / Lateralisiert / Dysplasisch) / Meije Duo zementierte Hüftschäfte, Linea Hüftschäfte und HLS Noetos Revision Knie-zementierte Schaftverlängerungen by Corin Medical Ltd.

Germany / BfArM · DEU · Apr 6, 2021

Key facts

Title Urgent Field Safety Notice for Oceane+ Hüftschäfte (Standard / Lateralisiert / Dysplasisch) / Meije Duo zementierte Hüftschäfte, Linea Hüftschäfte und HLS Noetos Revision Knie-zementierte Schaftverlängerungen by Corin Medical Ltd.
Regulator Germany / BfArM
Country DEU
Brand Oceane+ Hüftschäfte (Standard / Lateralisiert / Dysplasisch) / Meije Duo zementierte Hüftschäfte, Linea Hüftschäfte und HLS Noetos Revision Knie-zementierte Schaftverlängerungen
Manufacturer Corin Medical Ltd.
Models MARCH-21, 38330, REV02
Date Apr 6, 2021
Regulator page bfarm.de

At a glance

  • No Recall
  • No Field safety notice

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