FDANovember 14, 2019device

S.M.A.R.T. Nitinol Stent System and the S.M.A.R.T. Control Nitinol Stent System. The SMART stent system includes a self-expanding stent made of Nitinol (nickel-titanium alloy) material and a 6 French (2.0 mm) or 7 French (2.3 mm) sheathed delivery system. The stent is laser cut from a solid nitin...

Official recall recorded by the U.S. Food & Drug Administration.

The hazard

Cordis has initiated a labeling correction for S.M.A.R.T. and PRECISE stents due to incorrect MRI information on the IFU. The correct classification is "MRI Conditional" not "MRI Safe".

What to do

FDA enforcement status: Ongoing

Brands named

cardinal healthcardinal

Recall history

Other federal recalls tied to the same brand — a factual pattern, straight from the source data.

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