International safety notice

Portex Blue Line Ultra

Swiss / SwissMedic · CHE · Jul 28, 2008

Key facts

Title Portex Blue Line Ultra
Regulator Swiss / SwissMedic
Country CHE
Brand Portex Blue Line Ultra
Manufacturer Smiths Medical
Models B100833090, «M_1_Bezeichnung», «Name3», 1293475, 09.07.08, B100813090, «M_2_Charge», 830076-71-1, «M_2_Bezeichnung», B100813080, «M_2_ArtikelNr», 1293476 and 11 more
Event type Safety Notice
Date Jul 28, 2008
Regulator page fsca.swissmedic.ch

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

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