Medtronic Perfusion Systems: Medical Device Recall in 2025 - (Recall #: Z-0985-2025)

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:

EOPA Arterial Cannula, Model Numbers 77422 (22 Fr) and 77418 (18 Fr)

Product Classification:

Class II

Date Initiated: December 12, 2024

Date Posted: January 29, 2025

Recall Number: Z-0985-2025

Event ID: 96015

Reason for Recall:

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

Status: Ongoing

Product Quantity: 930 units

Code Information:

Model 77418 UDI-DI: 20763000135618, Lot Numbers: 2022041038; Model 77422 UDI-DI: 20643169485970, Lot Number: 2023020934

Distribution Pattern:

Worldwide - US Nationwide distribution.

Voluntary or Mandated:

Voluntary: Firm initiated