CardioQuip, LLC: Medical Device Recall in 2023 - (Recall #: Z-0566-2024)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2023.

Data Source: FDA.

Product Description:

CardioQuip Modular Cooler-Heater, Model: MCH-1000(m), Power: 115V-60Hz, 16A

Product Classification:

Class II

Date Initiated: October 24, 2023

Date Posted: December 27, 2023

Recall Number: Z-0566-2024

Event ID: 93446

Reason for Recall:

There is the potential that cooler-heater devices may contain bacterial contamination which could result in patient infection.

Status: Ongoing

Product Quantity: 2 units

Code Information:

UDI: 00860000846110 /Lot #:11160294 and 11161110

Distribution Pattern:

US: California, Texas, Pennsylvania, Washington, Ohio, Nebraska OUS: None

Voluntary or Mandated:

Voluntary: Firm initiated