Contego Medical, Inc.

12 devices · 71 adverse event reports · 8 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.

All Contego Medical, Inc. devices

• Neuroguard IEP® System NG-0740-140-2

  Stent, Carotid
  2 recalls32 reports
• Neuroguard IEP® System NG-NV-6-40

  Stent, Carotid
  2 recalls9 reports
• Neuroguard IEP® System NG-NV-7-40

  Stent, Carotid
  2 recalls8 reports
• Neuroguard IEP® System NG-0640-140-2

  Stent, Carotid
  2 recalls7 reports
• Neuroguard IEP® System NG-0730-140-2

  Stent, Carotid
  1 recall5 reports
• Neuroguard IEP® System NG-0630-140-2

  Stent, Carotid
  1 recall3 reports
• Neuroguard IEP® System NG-NV-6-30

  Stent, Carotid
  1 recall2 reports
• Neuroguard IEP® System NG-NV-7-30

  Stent, Carotid
  1 recall1 report
• Paladin 5x30

  Catheter, Angioplasty, Peripheral, Transluminal
  1 report
• Vanguard 6200x135

  Catheter, Angioplasty, Peripheral, Transluminal
  1 report
• Paladin 5.5x30

  Catheter, Angioplasty, Peripheral, Transluminal
  1 report
• Paladin 5.5.x20

  Catheter, Angioplasty, Peripheral, Transluminal
  1 report