International safety notice

Application Card software SynchroMed® II Implantable Drug Pump Model

Swiss / SwissMedic · CHE · Mar 19, 2012

Key facts

Title Application Card software SynchroMed® II Implantable Drug Pump Model
Regulator Swiss / SwissMedic
Country CHE
Brand Application Card software SynchroMed® II Implantable Drug Pump Model
Manufacturer Medtronic Inc.
Models CH-3053, 031‐868.01.30, 140.000, FA535, 868.0130, 12.3.2012
Event type Safety Notice
Date Mar 19, 2012
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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