Philips Medical Systems North America recalls

Philips Medical Systems North America appears in 5 official U.S. recall notices indexed by RecallRadar, most recently on 2014-03-26.

Company names are normalized from agency data (legal suffixes removed), so related firms may appear under separate pages.

• Philips Model EPIQ 5 Ultrasound System
  FDA Device · Class II · 2014-03-26 · Philips Medical Systems North America
• Philips HeartStart Home and OnSite (HS1) automated external defibrillators (AEDs)
  FDA Device · Class II · 2014-03-26 · Philips Medical Systems North America
• Philips Model EPIQ 7 Ultrasound System
  FDA Device · Class II · 2014-03-26 · Philips Medical Systems North America
• Philips HeartStart FR3 Automated External Defibrillator (AED), models 861388 and 861389
  FDA Device · Class II · 2014-03-26 · Philips Medical Systems North America
• EPIQ 7 Ultrasound System, Model 795200, 795201, 795202
  FDA Device · Class II · 2013-11-27 · Philips Medical Systems North America