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FDASeptember 23, 2016device

VIA 27 Microcatheter, Part No. FG27-154-01, Model No. VIA-27-154-01 The VIA 27 is intended for the introduction of non-liquid interventional devices (such as stents/flow diverters) and infusion of diagnostic (such as contrast media) or therapeutic agents into the neuro, peripheral, and coronary v...

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

The hazard

Sequent Medical is recalling the VIA 27 Microcatheter because it may not adequately re-sheath the interventional device into the catheter as designed.

What to do

FDA enforcement status: Terminated

Brands named

sequent medicalsequent

Recall history

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

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VIA 27 Microcatheter, Part No. FG27-154-01, Model No. VIA-27-154-01 The VIA 27 is intended for the introduction of non-liquid interventional devices (such as stents/flow diverters) and infusion of diagnostic (such as contrast media) or therapeutic agents into the neuro, peripheral, and coronary v... — Recall Details · AllClear