International safety notice

Urgent Field Safety Notice for Transplant-Aspiration Needle, SPI-CUT by Somatex Medical Technologies GmbH / Berlin

Germany / BfArM · DEU · Aug 21, 2018

Key facts

Title Urgent Field Safety Notice for Transplant-Aspiration Needle, SPI-CUT by Somatex Medical Technologies GmbH / Berlin
Regulator Germany / BfArM
Country DEU
Brand Transplant-Aspiration Needle, SPI-CUT
Manufacturer Somatex Medical Technologies GmbH / Berlin
Models 49581, 49998, 180635, 48811, 180845, 48763, 49122, 48916, 48915, 49895, 49668, 48679 and 55 more
Date Aug 21, 2018
Regulator page bfarm.de

At a glance

  • No Recall
  • No Field safety notice
  • 100–999 Matching device models in FDA data
  • 100–999 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

Browse all International device safety notices