FDAFebruary 21, 2023device

Biosense Webster Carto Vizigo Bi-Directional Guiding Sheath, 8.5F(Medium), REF D-1385-02-S, RX CE 2797, Sterile

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

The hazard

Incorrect labeling; specifically, the product name, lot number and product code on the carton label for Bi-Directional Guiding Sheaths does not match the inner label pouch

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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Biosense Webster Carto Vizigo Bi-Directional Guiding Sheath, 8.5F(Medium), REF D-1385-02-S, RX CE 2797, Sterile — Recall Details · AllClear