Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
VIA 27 Microcatheter Recalled by Sequent Medical Inc Due to Sequent Medical is recalling the VIA 27 Microcatheter...
What You Should Do
Stop using this product immediately. Do not consume, use, or distribute it.
Return the product to the place of purchase for a full refund. If you have questions, contact Sequent Medical Inc directly.
Affected Products
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 vasculature. The catheter is inserted into the body through a small puncture made in the skin and into a blood vessel. The VIA 27 Microcatheter is contraindicated for use with liquid embolic materials, such as n-butyl 2-cyanoacrylate or ethylene vinyl alcohol & DMSO (dimethyl sulfoxide).
Quantity: 618 units
Why Was This Recalled?
Sequent Medical is recalling the VIA 27 Microcatheter because it may not adequately re-sheath the interventional device into the catheter as designed.
Where Was This Sold?
This product was distributed to 11 states: CA, FL, KS, MD, MN, MO, NY, NC, OH, TN, WV
About Sequent Medical Inc
Sequent Medical Inc has 1 total recall tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report