International safety notice

Lot Recall for the Sarns™ Antegrade Cardioplegia Cannula, Terumo Europe NV

Germany / BfArM · DEU · Sep 18, 2012

Key facts

Title Lot Recall for the Sarns™ Antegrade Cardioplegia Cannula, Terumo Europe NV
Regulator Germany / BfArM
Country DEU
Brand the Sarns™ Antegrade Cardioplegia Cannula, Terumo Europe NV
Manufacturer Lot Recall for the Sarns™ Antegrade Cardioplegia Cannula, Terumo Europe NV
Models 0551294, 0558941, 0558280, 0596204, 0661142, 0607020, 0571584, 0574328, 0565841, 0618429, 0571163, FSN1207A and 93 more
Date Sep 18, 2012
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