FDASeptember 11, 2015device

One Step Button, Low Profile Initial Placement PEG Kit, gastro-enterostomy tube.

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

The hazard

Boston Scientific Corp. initiated a voluntary recall of specific lots of the EndoVive One Step Button, including the Decompression Tube and Low Profile Replacement Button devices because they may contain decompression tube adapters with a protrusion that could impede its ability to be introduced or removed from the PEG Button.

What to do

FDA enforcement status: Terminated

Brands named

boston scientificboston

Recall history

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

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