Medtronic Perfusion Systems: Medical Device Recall in 2025 - (Recall #: Z-0986-2025)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2025.

Data Source: FDA.

Product Description:

Select Series Angled Tip Arterial Cannula, Model Number 72422 (22 Fr)

Product Classification:

Class II

Date Initiated: December 12, 2024

Date Posted: January 29, 2025

Recall Number: Z-0986-2025

Event ID: 96015

Reason for Recall:

Incorrect labeling for seven manufactured lots of certain models of Arterial Cannulae.

Status: Ongoing

Product Quantity: 440 units

Code Information:

Model 72422 UDI-DI: 20643169485970, Lot Numbers: 2023071075, 202309C075

Distribution Pattern:

Worldwide - US Nationwide distribution.

Voluntary or Mandated:

Voluntary: Firm initiated