Medtronic Perfusion Systems: Medical Device Recall in 2020 - (Recall #: Z-2495-2020)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2020.

Data Source: FDA.

Product Description:

Extra corporeal circuit with bio-active surface.

Product Classification:

Class II

Date Initiated: August 8, 2018

Date Posted: July 15, 2020

Recall Number: Z-2495-2020

Event ID: 85821

Reason for Recall:

Affected products failed a sterilization test.

Status: Terminated

Product Quantity: 10 units

Code Information:

Lot# 215729283

Distribution Pattern:

Domestic Distribution only to CA and MI.

Voluntary or Mandated:

Voluntary: Firm initiated