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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
Recalled July 31, 2019 · FDA recall Z-2053-2019 · Zevex Incorporated (dba MOOG Medical Devices Group)
Hazard
Administration sets leaked at the filter. · FDA Class II
Units
569/20-set caess
Sold at
Distribution was made to GA, IL, KS, MA, MI, and OH. There was no foreign/military/government distribution.
Description
Administration sets leaked at the filter.
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 intravenous, intra-arterial, epidural, subcutaneous, or enteral infusions.
Manufacturer(s)
Zevex Incorporated (dba MOOG Medical Devices Group)
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →