International safety notice

Recall for Genesis II Femoral Components, Smith & Nephew

Germany / BfArM · DEU · May 11, 2009

Key facts

Title Recall for Genesis II Femoral Components, Smith & Nephew
Regulator Germany / BfArM
Country DEU
Brand Genesis II Femoral Components, Smith & Nephew
Manufacturer Recall for Genesis II Femoral Components, Smith & Nephew
Models 08AMU697, 02622541001, 2718832, DEUTDESS65, 71420010, DRESOEFF643, 71420012, 70075, N420062, 883200, 78532, IBU64380011 and 20 more
Date May 11, 2009
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

Browse all International device safety notices