FDAJune 29, 2022device

CARTO VIZIGO 8.5F Bi-Directional Guiding Sheath, REF: D138501. Used to introduce various cardiovascular catheters into the heart.

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

The hazard

Outside packaging for a device indicated for introducing cardiovascular catheters into the heart, sustained water damage, which may have affected the sterile barrier of the product inside. Devices with a compromised sterile barrier could be a source for infection.

What to do

FDA enforcement status: Ongoing

Brands named

biosense websterbiosense

UPCs

10846835016253

Recall history

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

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CARTO VIZIGO 8.5F Bi-Directional Guiding Sheath, REF: D138501. Used to introduce various cardiovascular catheters into the heart. — Recall Details · AllClear