MICROVENTION INC. recalls VIA Microcatheter VIA 21 REF VIA-21-154-01 - Product Usage: is a single lumen catheter designed to be introduced over a

Recalled June 16, 2021 · FDA recall Z-1829-2021 · MICROVENTION

Hazard

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

Units

N/A

Sold at

U.S. Nationwide distribution in the states of FL, IA, MI, MN, TN and TX.

Description

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

Product

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.

Manufacturer(s)

MICROVENTION INC.

Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →