FDAFebruary 16, 2024device

CARTO VIZIGO Bi-Directional Guiding Sheath, REF D128502 The CARTO VIZIGOTM Bi-Directional Guiding Sheath is designed to provide accessibility and maneuverability in the cardiac anatomy. The steerable sheath is fitted with a hemostasis valve to minimize blood loss during catheter introduction and/...

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

The hazard

Due to a manufacturing issue, device under process validation phase were inadvertently mixed into the main manufacturing process.

What to do

FDA enforcement status: Ongoing

Brands named

biosense websterbiosense

UPCs

10846835016277

Recall history

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

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