Arjo recalls

Arjo appears in 9 official U.S. recall notices indexed by RecallRadar, most recently on 2017-07-19.

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

• ArjoHuntleigh Flowtron ACS900, medical pump, software V1.099 Device is used to prevent the occurrence of Deep Vein Thrombosis (DVT) in at-r…
  FDA Device · Class II · 2017-07-19 · Arjo
• The Concerto Basic Shower Trolley is intended for assisted hygiene care, especially showering and bathing of residents in care environments…
  FDA Device · Class II · 2016-04-20 · Arjo
• Medium 2-Hooks Spreader Bar for use with Loop Slings, sizes small, medium and large on the Maxi Sky 2 Ceiling Lift
  FDA Device · Class II · 2014-10-22 · Arjo
• Enterprise 9000 Bed
  FDA Device · Class II · 2013-08-14 · Arjo
• Enterprise 8000 Bed
  FDA Device · Class II · 2013-08-14 · Arjo
• Flowtron Trio DVT Pump
  FDA Device · Class II · 2013-01-02 · Arjo
• Chorus Mobile Patient Lifter
  FDA Device · Class II · 2012-07-18 · Arjo
• Encore Mobile Patient Lifter
  FDA Device · Class II · 2012-07-18 · Arjo
• Sara Plus Mobile Patient Lifter
  FDA Device · Class II · 2012-07-18 · Arjo