International safety notice

Diagnostické zdravotnické prostředky in vitro

Czech / Ksrzis · CZE · Nov 30, 2017

Key facts

Title Diagnostické zdravotnické prostředky in vitro
Regulator Czech / Ksrzis
Country CZE
Brand Alinity i Processing Module
Manufacturer Abbott
Models AI01095, AI01101, AI01070, AI01126, AI01157, AI01079, AI01083, AI01032, AI01081, AI01169, AI01120, AI01172 and 72 more
Event type Safety Notice
Date Nov 30, 2017
Regulator page eregpublicsecure.ksrzis.cz

At a glance

  • No Recall
  • Yes 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