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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
Recalled March 7, 2018 · FDA recall Z-0698-2018 · Zevex Incorporated (dba Moog Medical Medical Devices Group)
Hazard
Particulate found on the Curlin spike. · FDA Class II
Units
756/20-administration set cases
Sold at
Distribution was nationwide. There was government and military distribution. Foreign distribution was made to Canada, Saudi Arabia, Turkey, Croatia, United Arab Emirates, and Australia.
Description
Particulate found on the Curlin spike.
Product
MOOG Curlin Infusion Administration Set, Ref 340-4133, Non-DEHP Microbore Tubing with Non-Vented Bag Spike and Needleless Injection Port (Positive Pressure), packaged 20/box, for use with the Moog Curlin Ambulatory Volumetric Infusion Pump, RX, Sterile. Product Usage: Administration set to be used with the Moog Curlin infusion Pump. The pump can be used for intravenous, intra-arterial, epidural, subcutaneous, or enteral infusions.
Manufacturer(s)
Zevex Incorporated (dba Moog Medical Medical Devices Group)
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →