Schiller AG

12 devices · 399 adverse event reports · 34 deaths reported · 7 devices named in recalls

Counts reflect reports that name each device's exact identifier. Larger companies sell more devices, so totals should not be read as a safety ranking.

• Tempus LS-MANUAL 3.940589

  Pacemaker, Cardiac, External Transcutaneous (Non-Invasive)
  4 recalls34 deaths391 reports
• ARGUS PB-3000 PB-3000 Var.7, sub-variant: SAG

  Monitor, Physiological, Patient(With Arrhythmia Detection Or Alarms)
  1 recall0 reports
• ARGUS PB-3000 PB-3000 Var.7, sub-variant: M/I

  Monitor, Physiological, Patient(With Arrhythmia Detection Or Alarms)
  1 recall0 reports
• CARDIOVIT AT-180 3.920570

  Electrocardiograph
  1 recall0 reports
• ARGUS PB-3000 PB-3000 Var.7, sub-variant: C

  Monitor, Physiological, Patient(With Arrhythmia Detection Or Alarms)
  1 recall0 reports
• ARGUS PB-3000 PB-3000 Var.8, sub-variant: Q

  Monitor, Physiological, Patient(With Arrhythmia Detection Or Alarms)
  1 recall0 reports
• ARGUS PB-3000 PB-3000 Var.9, sub-variant: Q

  Monitor, Physiological, Patient(With Arrhythmia Detection Or Alarms)
  1 recall0 reports
• SCHILLER BP-200 plus

  System, Measurement, Blood-Pressure, Non-Invasive
  3 reports
• ARGUS® PB-1000 3.920948

  Monitor, Physiological, Patient(With Arrhythmia Detection Or Alarms)
  2 reports
• Schiller ECG wire set 2.410308

  Cable, Transducer And Electrode, Patient, (Including Connector)
  1 report
• CARDIOVIT® FT-1 3.900863

  Electrocardiograph
  1 report
• ARGUS PB-3000 PB-3000 Var.10, sub-variant: M/I

  Monitor, Physiological, Patient(With Arrhythmia Detection Or Alarms)
  1 report