FDAJuly 3, 2019device

LivaNova SMART PERFUSION PACK INSPIRE 8S - Product Usage: The affected product is a perfusion tubing pack use in surgical procedures requiring extracorporeal support. The perfusion tubing packs include the cuvette used with equipment to monitor blood.

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

The hazard

Perfusion tubing pack was packaged with the incorrect cuvette.

What to do

FDA enforcement status: Terminated

Brands named

livanova

UPCs

00803622140136

Recall history

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

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