Cincinnati Sub-Zero Products LLC, a Gentherm Company: Medical Device Recall in 2019 - (Recall #: Z-0418-2020)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2019.

Data Source: FDA.

Product Description:

Blanketrol II Hyper-Hypothermia System, Models 222R and 222S - Product Usage: The system is composed of a heater, a compressor, a circulating pump and blankets/pads.

Product Classification:

Class II

Date Initiated: July 2, 2019

Date Posted: November 27, 2019

Recall Number: Z-0418-2020

Event ID: 83464

Reason for Recall:

Warnings statements have been added- exceeding 40 degree C for extended periods may cause tissue damage. Additionally, a caution was added and clarifications were made regarding the use of the Automatic modes

Status: Terminated

Product Quantity: 3726

Code Information:

Model 222R (071-18490 through 123-20534) Model 222S (104-2-00001 through 161-2-01848)

Distribution Pattern:

Worldwide distribution - US Nationwide and countries of Afghanistan, Argentina, Australia, Austria, Azerbaijan, Bahamas, Bahrain, Belgium, Bhutan, Brazil, Brunei, Canada Chile, China, Colombia, Costa Rica, Ecuador, Egypt, El Salvador, France, Germany, Guatemala, Hong Kong, India, Indonesia, Israel, Italy, Japan, Kazakhstan, Kenya, Kuwait, Lebanon, Malaysia, Mexico, Morocco, Nepal, Netherlands, New Zealand, Oman, Pakistan, Palestine, Panama, Philippines, Qatar, Saudi Arabia, Singapore, South Africa, South Korea, Spain, Taiwan, Thailand, Trinidad and Tobago, Turkey, United Arab Emirates, Venezuela, Vietnam.

Voluntary or Mandated:

Voluntary: Firm initiated