FDAMay 17, 2017device

PENTARAY NAV High-Density Mapping Catheter.

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

The hazard

Contraindication language updated in the Instructions For Use (IFU) to indicate that Pentaray Catheters should not be used in patients with prosthetic valves.

What to do

FDA enforcement status: Terminated

Brands named

biosense websterbiosense

UPCs

108468350095761084683500958310846835009590108468350096061084683500961310846835009620

Recall history

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

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