Medtronic Inc.: Medical Device Recall in 2024 - (Recall #: Z-1317-2024)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2024.

Data Source: FDA.

Product Description:

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

Product Classification:

Class II

Date Initiated: February 16, 2024

Date Posted: March 27, 2024

Recall Number: Z-1317-2024

Event ID: 94167

Reason for Recall:

There is a potential for sterile package breach.

Status: Ongoing

Product Quantity: 65 units

Code Information:

a) AB9U14080090, UDI/DI 00643169796294, Batch Number B456626; b) AB9U18100090, UDI/DI 00643169796409, Batch Number B456811; c) AB9G14100090, IUDI/DI 00763000547325, Batch Number B460542

Distribution Pattern:

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

Voluntary or Mandated:

Voluntary: Firm initiated