FDAJune 24, 2022device
UroLift System REF UL400-4, QTY 4 Urolfit System with Handle Release Tool
Official recall recorded by the U.S. Food & Drug Administration.
The hazard
There is the potential that during implant deployment, the device may not properly deliver a implant.
What to do
FDA enforcement status: Ongoing
Brands named
neotract
UPCs
0081493202004900814932020001
Recall history
Other federal recalls tied to the same brand — a factual pattern, straight from the source data.
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