FDAFebruary 20, 2024device

EndoVive 20Fr Push Safety PEG Kit (Box 2)-Indicated for enteral nutrition directly into the stomach in both pediatric and adult patients who are unable to consume nutrition by conventional means. UPN: M00566471

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

The hazard

Inability to advance the guidewire through the feeding tube during placement due to blocked lumen of the barb connector. May lead prolongation in the procedure to exchange the device for another leading to leading to a cascade of events which may include additional intervention to close the puncture site, bleeding, leakage of gastric contents, and aspiration

What to do

FDA enforcement status: Ongoing

Brands named

boston scientificboston

UPCs

08714729802631

Recall history

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

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