FDANovember 25, 2014device

TactiSys Quartz Pack, PN-004 400. For percutaneous catheter radiofrequency (RF) ablation of atrial cardiac arrhythmias that allows visualization of the contact force between TactiCath quartz catheter tip and the heart wall. Product Usage: This device is indicated for use in cardiac electrophysiol...

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

The hazard

A configuration update needs to be done on TactiSys to appropriately recognize all TactiCath catheters.

What to do

FDA enforcement status: Terminated

Brands named

st jude medical

Recall history

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

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TactiSys Quartz Pack, PN-004 400. For percutaneous catheter radiofrequency (RF) ablation of atrial cardiac arrhythmias that allows visualization of the contact force between TactiCath quartz catheter tip and the heart wall. Product Usage: This device is indicated for use in cardiac electrophysiol... — Recall Details · AllClear