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