FDADecember 18, 2023device

TactiFlex Ablation Sensor Enabled Ablation Catheter, Models A-TFSE-FJ, 7.5 F shaft and an 8F distal section, Sterile.

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

The hazard

When the catheters are used with the EnSiteX EP System, the system does not correctly recognize the catheter as the appropriate product model and instead reads and displays it as a different model. This results in some features specific to the catheter do not appear on the display and the catheter image may also appear inverted.

What to do

FDA enforcement status: Ongoing

Brands named

st jude medical atrial fibrillation division

UPCs

05415067034618

Recall history

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

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TactiFlex Ablation Sensor Enabled Ablation Catheter, Models A-TFSE-FJ, 7.5 F shaft and an 8F distal section, Sterile. — Recall Details · AllClear