International safety notice

Cappella

Swiss / SwissMedic · CHE · Nov 12, 2012

Key facts

Title Cappella
Regulator Swiss / SwissMedic
Country CHE
Brand Cappella
Manufacturer Liko AB
Models 4-8812357, 950542, DS122RD, 2027002, 950543, DS122_RD, 411555, DS121_RD, 7062132, DS121RD, 411000, 812-934-1348 and 12 more
Event type Safety Notice
Date Nov 12, 2012
Regulator page fsca.swissmedic.ch

At a glance

  • No Recall
  • Yes Field safety notice
  • 1–9 Matching device models 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