International safety notice

Recall for the products megro ID plus und megroCID, Megro GmbH & Co. KG

Germany / BfArM · DEU · Oct 30, 2014

Key facts

Title Recall for the products megro ID plus und megroCID, Megro GmbH & Co. KG
Regulator Germany / BfArM
Country DEU
Brand the products megro ID plus und megroCID, Megro GmbH & Co. KG
Manufacturer Recall for the products megro ID plus und megroCID, Megro GmbH & Co. KG
Models 28.10.2014, 007-1006, 007-1017, 003-1006, 99-23, 99-10, 003-0032, 007-3005, 003-3014, 99-37, 007-3010, 10588 and 35 more
Date Oct 30, 2014
Regulator page bfarm.de

At a glance

  • No Recall
  • No Field safety notice

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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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