International safety notice

Urgent Field Safety Notice for Angiodyn by PendraCare International

Germany / BfArM · DEU · Oct 21, 2019

Key facts

Title Urgent Field Safety Notice for Angiodyn by PendraCare International
Regulator Germany / BfArM
Country DEU
Brand Angiodyn
Manufacturer PendraCare International
Models 1904-0263, 4510778754, 5011527, 1906-0408, 3-7-2019, JL3.5, 4510580294, 27-05-2019, 4510769544, 5011644, 4510657793, 5011514 and 24 more
Date Oct 21, 2019
Regulator page bfarm.de

At a glance

  • No Recall
  • No Field safety notice
  • 1–9 Matching device models 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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