FDA Enforcement Class II Terminated

Blanketrol III Hyper-Hypothermia System- body hypothermia system temperature management Model 233 - Product Usage: The system is composed of a heater, a compressor, a circulating pump and blankets/pads.

Recall: Z-0417-2020 · Reported November 27, 2019

Enforcement

Recall Number
Z-0417-2020
Event ID
83464
Classification
Class II
Status
Terminated
Product Type
Devices
Firm
Cincinnati Sub-Zero Products LLC, a Gentherm Company
Voluntary / Mandated
Voluntary: Firm initiated
Initial Notification
Letter
Report Date
November 27, 2019
Initiation Date
July 2, 2019
Classification Date
November 18, 2019
Termination Date
June 22, 2020
Address
12011 Mosteller Rd, N/A, Cincinnati, OH, 45241-1528, United States

Description

Blanketrol III Hyper-Hypothermia System- body hypothermia system temperature management Model 233 - Product Usage: The system is composed of a heater, a compressor, a circulating pump and blankets/pads.

Reason

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

Code Info

Serial Numbers: 071-3-00123 through193-3-09498

Distribution

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.

Quantity

3932