Medtronic Inc. recalls Medtronic Abre Venous Self-expanding Sent System, Catalog nu
Recalled Product
Medtronic Abre Venous Self-expanding Sent System, Catalog number REF AB9U16080090 - Product Usage: intended for use in the iliofemoral veins for the treatment of symptomatic venous outflow obstruction.
Hazard / Issue
Incorrect size printed on the device; packaging is labeled correctly.
Issued by
FDA
Distribution: Nationwide (United States)
Lot/Code Info: UDI 00643169796348, Lot Number B086915
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