Atricure Inc: Medical Device Recalls in 2013

Updated on March 25, 2026.

According to to data from the FDA, there was 1 medical device recall made by Atricure Inc in 2013. See the detail of the recall below.

You can see similar recalls for other firms.

Data Source: FDA.

See this for other years:

Atricure Inc., Max1 Isolator Transpolar Pen. Model A000163. Used to ablate cardiac tissues during cardiac surgery using radiofrequency energy when connected to the AtriCure Ablation and Sensing Unit or for temporary cardiac pacing, sensing, recording, and stimulation during the evaluation of cardiac arrhythmias during surgery when connected to a temporary external cardiac pacemaker or recording device.