International safety notice

Recall for a surgical kit for femoropopliteal bypass surgery, Mölnlycke Health Care

Germany / BfArM · DEU · Dec 10, 2010

Key facts

Title Recall for a surgical kit for femoropopliteal bypass surgery, Mölnlycke Health Care
Regulator Germany / BfArM
Country DEU
Brand femoropopliteal bypass surgery, Mölnlycke Health Care
Manufacturer Recall for a surgical kit for femoropopliteal bypass surgery, Mölnlycke Health Care
Models 09237283, 10260332, 09283232, 09178080, 09457403, 09401563, 97002840-11, 10161767, 09442517, 2311111, 10230808, 09206315 and 9 more
Date Dec 10, 2010
Regulator page bfarm.de

At a glance

  • No Recall
  • No Field safety notice

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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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