FDAApril 21, 2021device

VIA Microcatheter VIA 21 REF VIA-21-154-01 - Product Usage: is a single lumen catheter designed to be introduced over a steerable guidewire into the vasculature.

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

The hazard

Due to inadvertently shipping to U.S. customers with international labeling which has some differences with US-cleared labeling.

What to do

FDA enforcement status: Terminated

Brands named

microvention

UPCs

00842429101650

Recall history

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

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