MICROVENTION INC.: Medical Device Recall in 2021 - (Recall #: Z-1829-2021)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2021.

Data Source: FDA.

Product Description:

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.

Product Classification:

Class III

Date Initiated: April 21, 2021

Date Posted: June 16, 2021

Recall Number: Z-1829-2021

Event ID: 88024

Reason for Recall:

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

Status: Terminated

Product Quantity: N/A

Code Information:

Catalog Number: VIA-21-154-01 UDI: (01)00842429101650(11)191104(17)221031(10)19110403M Lot Number: 19110403M

Distribution Pattern:

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

Voluntary or Mandated:

Voluntary: Firm initiated