International safety notice

Lot Recall of two products for the paediatric infusion, Smiths Medical Deutschland GmbH

Germany / BfArM · DEU · Apr 20, 2010

Key facts

Title Lot Recall of two products for the paediatric infusion, Smiths Medical Deutschland GmbH
Regulator Germany / BfArM
Country DEU
Brand the paediatric infusion, Smiths Medical Deutschland GmbH
Manufacturer Lot Recall of two products for the paediatric infusion, Smiths Medical Deutschland GmbH
Models 0-85630, 29259-314, 04.03.2010, 23.03.2010, 04-0030, 2042±472, 25.02.2010, N256472, 1-97-11A-077A, 1721057, 204256472, 1723448 and 10 more
Date Apr 20, 2010
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