International safety notice

Urgent Field Safety Notice for cobas p501 post-analytical unit and cobas p701 post-analytical unit by Roche Diagnostics GmbH

Germany / BfArM · DEU · Apr 10, 2019

Key facts

Title Urgent Field Safety Notice for cobas p501 post-analytical unit and cobas p701 post-analytical unit by Roche Diagnostics GmbH
Regulator Germany / BfArM
Country DEU
Brand cobas p501 post-analytical unit and cobas p701 post-analytical unit
Manufacturer Roche Diagnostics GmbH
Models 20-MAR-2019, 05158494001, 30-SEPTEMBER-2019, 05349966001, SBN-SIS-2019-002
Date Apr 10, 2019
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

Browse all International device safety notices