Zevex Dba Moog Medical Medical Devices Group recalls

Zevex Dba Moog Medical Medical Devices Group appears in 6 official U.S. recall notices indexed by RecallRadar, most recently on 2018-03-07.

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

• MOOG Curlin Infusion Administration Set, Ref 340-4134, Non-DEHP Microbore Tubing with Non-Vented Bag Spike and Y-Site with Check Valve, pac…
  FDA Device · Class II · 2018-03-07 · Zevex Dba Moog Medical Medical Devices Group
• MOOG Curlin Infusion Administration Set, Ref 340-4168, Non-DEHP Microbore Tubing with Non-Vented Bag Spike and distal Female Luer Y-Site wi…
  FDA Device · Class II · 2018-03-07 · Zevex Dba Moog Medical Medical Devices Group
• MOOG Curlin Infusion Administration Set, Ref 340-4166, Non-DEHP Microbore Tubing with Non-Vented Spike, Anti-Siphon Valve included for Free…
  FDA Device · Class II · 2018-03-07 · Zevex Dba Moog Medical Medical Devices Group
• MOOG Curlin Infusion Administration Set, Ref 340-4133, Non-DEHP Microbore Tubing with Non-Vented Bag Spike and Needleless Injection Port (P…
  FDA Device · Class II · 2018-03-07 · Zevex Dba Moog Medical Medical Devices Group
• MOOG Curlin Infusion Administration Set, Ref 340-4114, Non-DEHP Microbore Tubing with Non-Vented Bag Spike, packaged 20/box, for use with t…
  FDA Device · Class II · 2018-03-07 · Zevex Dba Moog Medical Medical Devices Group
• MOOG Curlin Infusion Administration Set, Ref 340-4169, Non-DEHP Microbore Tubing with Non-Vented Bag Spike and distal Ultrasite Needleless…
  FDA Device · Class II · 2018-03-07 · Zevex Dba Moog Medical Medical Devices Group