The Recall Desk

FDA (Devices) recall action 82864

Zevex Incorporated (dba MOOG Medical Devices Group) recalled 2 products on 2019-07-31

The FDA (Devices) publishes a recall like this one as 2 separate product records. They share a firm, a date and a cause; this page is all of them in one place, so the scale of the action is visible rather than spread across 2 pages.

Products
2
Announced
2019-07-31
Critical
0
Units
—

Why these products were recalled

Administration sets leaked at the filter.

The agency’s own wording, quoted from the enforcement report.

States named across these recalls

1–2 of 2

  • HighFDA (Devices)··2019-07-31

    MOOG Curlin Infusion Administration Sets Recalled for Filter Leaks

    Zevex Incorporated is recalling specific lots of MOOG Curlin Infusion Administration Sets because they leaked at the filter.

    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.
    Category
    Distribution
    6 states
  • HighFDA (Devices)··2019-07-31

    MOOG Curlin Infusion Administration Set Recalled for Filter Leaks

    Zevex Incorporated is recalling MOOG Curlin Infusion Administration Sets because they leaked at the filter. The affected sterile sets were distributed to six US states.

    Product
    MOOG Curlin Infusion Administration Set, REF 340-4130, Non-DEHP Tubing with Non-Vented Bag Spike and Vented 0.2 Micron Filter, packaged 20 sets/carton, sterile. Product Usage: Administration set to be used with the Moog Curlin Infusion Pump. The pump can be used for intraveno
    Category
    Distribution
    6 states