FDADecember 10, 2014device

Covidien Trellis-6 Peripheral Infusion System. Models BVT608010V01, BVT608030V01, BVT612010V01, and BVT612030V01. Sterile EO. Product Usage: Intended for controlled and selective infusion of physician-specified fluids, including thrombolytics, into the peripheral vasculature.

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

The hazard

A manufacturing error resulted in the risk of incorrect proximal and distal balloon inflation port identification on the units. Units have been identified to have the distal balloon inflation port incorrectly labeled as proximal, and, the proximal balloon port incorrectly labeled as distal.

What to do

FDA enforcement status: Terminated

Brands named

covidien

Recall history

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

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