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Recall Observatory FDA recall evidence

Device 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.

Z-0615-2013

December 10, 2012

Class II

Product summary

Firm
Arjo, Inc. dba ArjoHuntleigh
Event
Event 63857
Status
Terminated
Classification
Class II
Quantity
2,859 unts
Official record key
device-enforcement:Z-0615-2013

Official wording

Reason: The Flowtron Trio DVT Pump has been marketed without proper FDA Approval.

Code information: Model 512003, all serial numbers

Distribution pattern: 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.

Derived failure modes

  • Unknown

    reason.no_named_rule · v1.0.0

    The Flowtron Trio DVT Pump has been marketed without proper FDA Approval.