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Arjo, Inc. dba ArjoHuntleigh recalls Flowtron Trio DVT Pump; an Rx intermittent pneumatic compression deep vein thrombosis pump; ArjoHuntleigh AB, Eslov, Swe
Recalled January 2, 2013 · FDA recall Z-0615-2013 · Arjo, Inc.
Hazard
The Flowtron Trio DVT Pump has been marketed without proper FDA Approval. · FDA Class II
Units
2,859 unts
Sold at
USA (nationwide) including the states of Alabama, Arkansas, Arizona, California, Colorado, Connecticut, Florida, Georgia, Iowa, Idaho, Illinois, Indiana, Kansas, Kentucky, Maryland, Maine, Michigan, Minnesota, Missouri, Mississippi, Montana, North Dakota, New Jersey, New York, Ohio, Oklahoma, Oregon, Pennsylvania, South Dakota, Tennessee, Texas, Utah, Virginia, Washington, Wisconsin and Wyoming.
Description
The Flowtron Trio DVT Pump has been marketed without proper FDA Approval.
Product
Flowtron Trio DVT Pump; an Rx intermittent pneumatic compression deep vein thrombosis pump; ArjoHuntleigh AB, Eslov, Sweden; Model 512003; a non-invasive prophylaxis system for reducing the incidence of deep vein thrombosis.
Manufacturer(s)
Arjo, Inc. dba ArjoHuntleigh
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →