International safety notice

Ανάκληση των παρτίδων CHF002057 και CHF002112 του in vitro διαγνωστικού ιατροτεχνολογικού προϊόντος Unyvero BCU Blood Culture Cartridge Set Για να δείτε την απόφαση πατήστε εδώ

Greece / EOF · GRC · Mar 29, 2017

Key facts

Title Ανάκληση των παρτίδων CHF002057 και CHF002112 του in vitro διαγνωστικού ιατροτεχνολογικού προϊόντος Unyvero BCU Blood Culture Cartridge Set Για να δείτε την απόφαση πατήστε εδώ
Regulator Greece / EOF
Country GRC
Models 21006, CHF002057, DE-BFARM-2017-03-07-1993, 15562, 15125, 13-03-2017, 2106549500, Ν.1316, 2132040435, Ν.3730, CHF002112
Event type Recall, Safety Notice
Date Mar 29, 2017
Regulator page eof.gr

At a glance

  • Yes Recall
  • Yes Field safety notice
  • 10–99 Matching device models in FDA data
  • 10–99 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