Medtronic Inc. recalls Abre Venous Self-expanding Stent System, Product Numbers: a) AB9U14080090; b) AB9U18100090; c) AB9G14100090

Recalled March 27, 2024 · FDA recall Z-1317-2024 · Medtronic

Hazard

There is a potential for sterile package breach. · FDA Class II

Units

65 units

Sold at

Worldwide distribution - US Nationwide and the countries of Australia, Canary Islands, Colombia, Finland, Germany, Netherlands, Portugal, Spain, Switzerland, United Arab Emirates, United Kingdom.

Description

There is a potential for sterile package breach.

Product

Abre Venous Self-expanding Stent System, Product Numbers: a) AB9U14080090; b) AB9U18100090; c) AB9G14100090

Manufacturer(s)

Medtronic Inc.

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