International safety notice

Urgent field safety notice for Eclipse Injection Needle, Eclipse Injection Needle with Luer-Lok Syringe and Preset Eclipse Arterial Blood Collection Syringe, BD Medical EEMA / BD Preanalytical Systems EEMA

Germany / BfArM · DEU · Jan 17, 2017

Key facts

Title Urgent field safety notice for Eclipse Injection Needle, Eclipse Injection Needle with Luer-Lok Syringe and Preset Eclipse Arterial Blood Collection Syringe, BD Medical EEMA / BD Preanalytical Systems EEMA
Regulator Germany / BfArM
Country DEU
Brand Eclipse Injection Needle, Eclipse Injection Needle with Luer-Lok Syringe and Preset Eclipse Arterial Blood Collection Syringe, BD Medical EEMA / BD Preanalytical Systems EEMA
Manufacturer Urgent field safety notice for Eclipse Injection Needle, Eclipse Injection Needle with Luer-Lok Syringe and Preset Eclipse Arterial Blood Collection Syringe, BD Medical EEMA / BD Preanalytical Systems EEMA
Models 305793, 305784, MSS-16837B-FA, 305757, 364389, NEEDLE22GX1-1, 23GX1, 305781, 364390, 21X1-1, 30GX1, 22GX1-1 and 13 more
Date Jan 17, 2017
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

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