Recorder, event, implantable cardiac, (with arrhythmia detection)

FDA product code MXD · Class 2 · 13 devices · 9,185 reports · 6 devices named in recalls

• LINQ II™ LNQ22

  Medtronic, Inc. · Recorder, event, implantable cardiac, (with arrhythmia detection)
  2 recalls5,709 reports
• LINQ II™ LNQ22

  Medtronic, Inc. · Recorder, event, implantable cardiac, (with arrhythmia detection)
  1 recall1,228 reports
• BioMonitor III 436066

  BIOTRONIK SE & Co. KG · RECORDER,EVENT,IMPLANTABLE CARDIAC,(WITH ARRHYTHMIA DETECTION)
  655 reports
• LUX-Dx II+™ 60M312-100

  Boston Scientific Corporation · Recorder, event, implantable cardiac, (with arrhythmia detection)
  1 recall429 reports
• LUX-Dx™ Insertable Cardiac Monitor M301

  Boston Scientific Corporation · Recorder, event, implantable cardiac, (with arrhythmia detection)
  478 reports
• BioMonitor IIIm 450218

  BIOTRONIK SE & Co. KG · Recorder, event, implantable cardiac, (with arrhythmia detection)
  373 reports
• BioMonitor 2-AF 398493

  BIOTRONIK SE & Co. KG · RECORDER,EVENT,IMPLANTABLE CARDIAC,(WITH ARRHYTHMIA DETECTION)
  151 reports
• LUX-Dx II™ 60M302-100

  Boston Scientific Corporation · Recorder, event, implantable cardiac, (with arrhythmia detection)
  1 recall77 reports
• BioMonitor IV 471155

  BIOTRONIK SE & Co. KG · Recorder, Event, Implantable Cardiac, (With Arrhythmia Detection)
  82 reports
• LATITUDE® Clarity 7260

  Boston Scientific Corporation · Recorder, event, implantable cardiac, (with arrhythmia detection)
  1 recall0 reports
• myLUX™ Patient App 2939

  Boston Scientific Corporation · Recorder, event, implantable cardiac, (with arrhythmia detection)
  1 recall0 reports
• Assert-IQ™ DM5100

  St. Jude Medical, Inc. · Recorder, event, implantable cardiac, (with arrhythmia detection)
  2 reports
• Remote Assistant III 435292

  BIOTRONIK SE & Co. KG · RECORDER,EVENT,IMPLANTABLE CARDIAC,(WITH ARRHYTHMIA DETECTION)
  1 report