FDAMay 23, 2019device
DOSI-FUSER 12591 5-500D1 -USA, 12591 5-600D1 -USA Provide parenteral drug infusions at a constant flow without impeding patient mobility
Official recall recorded by the U.S. Food & Drug Administration.
The hazard
The product lacks 510(k) clearance, and therefore is misbranded and must be removed from the U.S. market.
What to do
FDA enforcement status: Terminated
Brands named
leventon s a uleventon
UPCs
0843602076747008436020768026
Recall history
No related federal recalls on record for this brand yet.
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