International safety notice

Recall for Fogarty Fortis Catheters, Edwards

Germany / BfArM · DEU · Jul 15, 2008

Key facts

Title Recall for Fogarty Fortis Catheters, Edwards
Regulator Germany / BfArM
Country DEU
Brand Fogarty Fortis Catheters, Edwards
Manufacturer Recall for Fogarty Fortis Catheters, Edwards
Models 58323513, 11-27, 949.250.2525, 2008-06-23, 58326739, 58326740, 58329130, 58329131, 58320652, 58326741, 949.250.2500, 58323511 and 6 more
Date Jul 15, 2008
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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