Arrow International Division recalls

Arrow International Division appears in 9 official U.S. recall notices indexed by RecallRadar, most recently on 2016-03-16.

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

• Percutaneous Insertion Tray
  FDA Device · Class I · 2016-03-16 · Arrow International Division
• FiberOptix Ultra 8 IAB: 8Fr 30cc The Arrow¿ IAB is utilized for intra aortic balloon counterpulsation therapy in the aorta, whereby balloon…
  FDA Device · Class I · 2016-03-16 · Arrow International Division
• UltraFlex IAB: 7.5Fr 30cc
  FDA Device · Class I · 2016-03-16 · Arrow International Division
• Percutaneous Insertion Tray
  FDA Device · Class I · 2016-03-16 · Arrow International Division
• UltraFlex IAB: 7.5Fr 40cc
  FDA Device · Class I · 2016-03-16 · Arrow International Division
• Ultra 8 IAB: 8Fr 30cc
  FDA Device · Class I · 2016-03-16 · Arrow International Division
• RediGuard IAB: 7Fr 30cc
  FDA Device · Class I · 2016-03-16 · Arrow International Division
• Ultra 8 IAB: 8Fr 40cc
  FDA Device · Class I · 2016-03-16 · Arrow International Division
• FiberOptix Ultra 8 IAB: 8Fr 40cc
  FDA Device · Class I · 2016-03-16 · Arrow International Division