Sequent Medical Inc: Medical Device Recalls in 2016

Updated on March 25, 2026.

According to to data from the FDA, there was 1 medical device recall made by Sequent Medical Inc in 2016. See the detail of the recall below.

You can see similar recalls for other firms.

Data Source: FDA.

See this for other years:

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).