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Zevex Incorporated (dba Moog Medical Medical Devices Group) Recalls
6 recalls on record · March 7, 2018 to March 7, 2018 · Medical Devices
March 7, 2018Medical DevicesFDA
Zevex Incorporated (dba Moog Medical Medical Devices Group) recalls MOOG Curlin Infusion Administration Set, Ref 340-4169, Non-DEHP Microbore Tubing with Non-Vented Bag Spike and distal Ul
Hazard: Particulate found on the Curlin spike.
March 7, 2018Medical DevicesFDA
Zevex Incorporated (dba Moog Medical Medical Devices Group) recalls MOOG Curlin Infusion Administration Set, Ref 340-4168, Non-DEHP Microbore Tubing with Non-Vented Bag Spike and distal Fe
Hazard: Particulate found on the Curlin spike.
March 7, 2018Medical DevicesFDA
Zevex Incorporated (dba Moog Medical Medical Devices Group) recalls MOOG Curlin Infusion Administration Set, Ref 340-4166, Non-DEHP Microbore Tubing with Non-Vented Spike, Anti-Siphon Valv
Hazard: Particulate found on the Curlin spike.
March 7, 2018Medical DevicesFDA
Zevex Incorporated (dba Moog Medical Medical Devices Group) recalls MOOG Curlin Infusion Administration Set, Ref 340-4134, Non-DEHP Microbore Tubing with Non-Vented Bag Spike and Y-Site wi
Hazard: Particulate found on the Curlin spike.
March 7, 2018Medical DevicesFDA
Zevex Incorporated (dba Moog Medical Medical Devices Group) recalls MOOG Curlin Infusion Administration Set, Ref 340-4133, Non-DEHP Microbore Tubing with Non-Vented Bag Spike and Needleles
Hazard: Particulate found on the Curlin spike.
March 7, 2018Medical DevicesFDA
Zevex Incorporated (dba Moog Medical Medical Devices Group) recalls MOOG Curlin Infusion Administration Set, Ref 340-4114, Non-DEHP Microbore Tubing with Non-Vented Bag Spike, packaged 20/
Hazard: Particulate found on the Curlin spike.