International safety notice

Lot recall of application systems KS and Multi APS, Cardea GmbH & Co. KG

Germany / BfArM · DEU · Jan 4, 2017

Key facts

Title Lot recall of application systems KS and Multi APS, Cardea GmbH & Co. KG
Regulator Germany / BfArM
Country DEU
Brand Lot recall of application systems KS and Multi APS, Cardea GmbH & Co. KG
Manufacturer Lot recall of application systems KS and Multi APS, Cardea GmbH & Co. KG
Models 1607001, BE002, 1549003, 1613004, 1637006, 1619001, 1638018, 1545004, 1637010, 1635006, 1638001, 2580433N and 60 more
Date Jan 4, 2017
Regulator page bfarm.de

At a glance

  • No Recall
  • No Field safety notice
  • 1–9 Matching device models in FDA data
  • 1–9 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