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Zevex Incorporated (dba MOOG Medical Devices Group) Recalls
2 recalls on record · July 31, 2019 to July 31, 2019 · Medical Devices
July 31, 2019Medical DevicesFDA
Zevex Incorporated (dba MOOG Medical Devices Group) recalls MOOG Curlin Infusion Administration Set, REF 340-4130-V, Non-DEHP Tubing with Non-Vented Bag Spike and Vented 0.2 Micron
Hazard: Administration sets leaked at the filter.
July 31, 2019Medical DevicesFDA
Zevex Incorporated (dba MOOG Medical Devices Group) recalls MOOG Curlin Infusion Administration Set, REF 340-4130, Non-DEHP Tubing with Non-Vented Bag Spike and Vented 0.2 Micron F
Hazard: Administration sets leaked at the filter.