Medtronic Perfusion Systems: Medical Device Recall in 2015 - (Recall #: Z-2420-2015)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2015.

Data Source: FDA.

Product Description:

Medtronic EOPA Arterial Cannula, Model # 77620. Lot: 2015060544 intended to deliver oxygenated blood to the heart during cardiopulmonary bypass procedures for up to 6 hours in duration.

Product Classification:

Class II

Date Initiated: July 24, 2015

Date Posted: August 26, 2015

Recall Number: Z-2420-2015

Event ID: 71897

Reason for Recall:

EOPA Arterial Cannula Devices in this lot were shipped without the guidewire.

Status: Terminated

Product Quantity: 221 (111 US, 110 OUS)

Code Information:

Lot number 2015060544;

Distribution Pattern:

Worldwide distribution. US nationwide including: FL, GA, IL, MI, NY, NC, PA, WV; Germany, Hong Kong, and Italy.

Voluntary or Mandated:

Voluntary: Firm initiated