FDAMarch 23, 2020device

Triever20 Aspiration Guide Catheter a component of FlowTriever Retrieval/ Aspiration System, UDI: 00850291007079

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

The hazard

The hemostasis valve of aspiration guide catheter devices may fail to seal resulting in a loss of vacuum during thrombus aspiration, which may result the procedure being prolonged as another device must be used or suboptimal thrombus removal if the problem is not detected.

What to do

FDA enforcement status: Terminated

Brands named

inari medicalinari

UPCs

00850291007079

Recall history

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

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