International safety notice

Urgent Field Safety Notice for Arrow Multiple-Lumen Catheter by Teleflex Medical USA

Germany / BfArM · DEU · Mar 18, 2020

Key facts

Title Urgent Field Safety Notice for Arrow Multiple-Lumen Catheter by Teleflex Medical USA
Regulator Germany / BfArM
Country DEU
Brand Arrow Multiple-Lumen Catheter
Manufacturer Teleflex Medical USA
Models 71F19L2688, 71F19L0818, DE-14702-UW1, COMO-27702, CE-15802, 14370773, 71F19L1885, 71F19L0807, CV-12712-FR1, DK-24702-EK, 71F19L1532, EIF-000413 and 6 more
Date Mar 18, 2020
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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