FDANovember 17, 2020device

Lotus Edge Valve System, Transcatheter Aortic Valve Prosthesis Premounted on Delivery System, 23mm, sterile, REF H749LVSUS230, GTIN 08714729960904

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

The hazard

Failure to execute the visual inspection correctly prior to locking the valve during the deployment process can lead to the inability to release the delivery system.

What to do

FDA enforcement status: Terminated

Brands named

boston scientificboston

UPCs

08714729960904

Recall history

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

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