FDAApril 17, 2015device

WEBSTER HIS Catheter, 4 Pole Fixed Curve with Auto ID Technology, for mapping of cardiac structure; i.e., stimulation and recording only. Catalog No: 01085413

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

The hazard

The Webster HIS catheter, 4Pole Fixed Curve with Auto ID, is not being recognized by the CARTO 3 navigation System.

What to do

FDA enforcement status: Terminated

Brands named

biosense websterbiosense

Recall history

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

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