Medtronic Inc., Cardiac Rhythm and Heart Failure (CRHF) recalls Instructions for Use for all model numbers of the Medtronic
Recalled Product
Instructions for Use for all model numbers of the Medtronic Abre Venous Self-Expanding Stent System.
Hazard / Issue
There have been reports of stent migration.
Issued by
FDA
Distribution: Nationwide (United States)
Lot/Code Info: The IFU for all model numbers and serial numbers.
View official government recall
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