FDAFebruary 26, 2021device

Biosense Webster, CARTO VIZIGO, Bi-Directional Guiding Sheath, 8.5F (Large) C3, REF: D138503, Rx Only, CE 2797, STERILE EO, udi: (01)10846835016260 - Product Usage: provide accessibility and maneuverability in the cardiac anatomy during cardiac electrophysiological mapping and ablation procedures.

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

The hazard

There is a potential for the hemostatic valve to dislodge while introducing the dilator or device into the sheath. This could result in minor bleeding and/or embolism

What to do

FDA enforcement status: Completed

Brands named

biosense websterbiosense

UPCs

10846835016260

Recall history

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

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