Reported Jan 2, 2013 · Terminated
Flowtron Trio DVT Pump; an Rx intermittent pneumatic compression deep vein thrombosis pump; ArjoHuntleigh AB, Eslov,…
Arjo, Inc. dba ArjoHuntleigh
Moderate riskThis product could cause temporary or reversible health problems — stop using it.What you should do
Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.
Firm contact: Arjo, Inc. dba ArjoHuntleigh · 2349 W Lake St · Addison, IL · 60101-6183
Is this the product you have?
- 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.
- Lot codes and dates
- Model 512003, all serial numbers
- Amount recalled
- 2,859 unts
Where it was sold
Why it was recalled
The Flowtron Trio DVT Pump has been marketed without proper FDA Approval.
This product could cause temporary or reversible health problems — stop using it.
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The guide adds the identifying codes laid out for scanning, symptoms to watch for, a timeline, and news coverage of this recall.
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