Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Flowtron Trio DVT Pump Recalled by Arjo, Inc. dba ArjoHuntleigh Due to The Flowtron Trio DVT Pump has been marketed...
What You Should Do
Stop using this product immediately. Do not consume, use, or distribute it.
Return the product to the place of purchase for a full refund. If you have questions, contact Arjo, Inc. dba ArjoHuntleigh directly.
Affected Products
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.
Quantity: 2,859 unts
Why Was This Recalled?
The Flowtron Trio DVT Pump has been marketed without proper FDA Approval.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Arjo, Inc. dba ArjoHuntleigh
Arjo, Inc. dba ArjoHuntleigh has 9 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report