FDAMay 7, 2018device

WaveCrest Left Atrial Appendage (LAA), Occlusion System (32 mm), Catalog Numbers WCR1523 and WCR2523.

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

The hazard

When attempting to recapture the 32-mm device, the tip of the delivery sheath may fold or buckle, resulting in increased retraction force and difficulty or failure to recapture the device.

What to do

FDA enforcement status: Terminated

Brands named

biosense websterbiosense

Recall history

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

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WaveCrest Left Atrial Appendage (LAA), Occlusion System (32 mm), Catalog Numbers WCR1523 and WCR2523. — Recall Details · AllClear