International safety notice

Aesculap recalls Columbus CR Femoral Components

Germany / BfArM · DEU · Jan 10, 2005

Key facts

Title Aesculap recalls Columbus CR Femoral Components
Regulator Germany / BfArM
Country DEU
Brand Aesculap recalls Columbus CR Femoral Components
Manufacturer Aesculap recalls Columbus CR Femoral Components
Models D-78532, NN007K, 2004-11-23, D-78501, 21060, 95-2922, 00028, 2004-1, 51196225, 78532, NN167K
Date Jan 10, 2005
Regulator page bfarm.de

At a glance

  • No Recall
  • No 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

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