International safety notice

Recall for InterGard Knitted vascular graft, Intervascular S.A.S.

Germany / BfArM · DEU · Jan 28, 2010

Key facts

Title Recall for InterGard Knitted vascular graft, Intervascular S.A.S.
Regulator Germany / BfArM
Country DEU
Brand InterGard Knitted vascular graft, Intervascular S.A.S.
Manufacturer Recall for InterGard Knitted vascular graft, Intervascular S.A.S.
Models 40199075, INTERVASCU1AR, 15705, 13705, E09198, IGK0008-40, 09J17
Date Jan 28, 2010
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