medical Class II Updated 2019-07-31

Zevex Incorporated (dba MOOG Medical Devices Group) recalls MOOG Curlin Infusion Administration Set, REF 340-4130-V, Non

Recalled Product

MOOG Curlin Infusion Administration Set, REF 340-4130-V, Non-DEHP Tubing with Non-Vented Bag Spike and Vented 0.2 Micron Filter with add-on check valve, packaged 20 sets/carton, sterile. The firm name on the label is ZEVEX, Inc., Salt Lake City, UT.


Hazard / Issue

Administration sets leaked at the filter.

Issued by

FDA

Affected States: GA, IL, KS, MA, MI, OH
Lot/Code Info: Lot numbers CF1820216, CF1821617, CF1822214, and CF1823616, UDI 38148440000471.
View official government recall

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