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

Hazard

There is a potential for sterile package breach.

Details from the source

Reason for recall: There is a potential for sterile package breach. Distribution: Worldwide distribution - US Nationwide and the countries of Australia, Canary Islands, Colombia, Finland, Germany, Netherlands, Portugal, Spain, Switzerland, United Arab Emirates, United Kingdom. Quantity: 65 units Lot/code info: a) AB9U14080090, UDI/DI 00643169796294, Batch Number B456626; b) AB9U18100090, UDI/DI 00643169796409, Batch Number B456811; c) AB9G14100090, IUDI/DI 00763000547325, Batch Number B460542

UPC codes

00643169796294, 00643169796409, 00763000547325

Source

Official record: FDA (Device enforcement) ↗

Republished from the official source above; details can change — the source record controls.