Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Electri-Cool II Portable Cold Therapy Unit Recalled by Gentherm Medical, LLC Due to This recall has been initiated to provide a...
What You Should Do
Stop using this product immediately. Do not consume, use, or distribute it.
Return the product to the place of purchase for a full refund. If you have questions, contact Gentherm Medical, LLC directly.
Affected Products
Electri-Cool II Portable Cold Therapy Unit, Model Number 767, Part Number 86193
Quantity: 484 devices
Why Was This Recalled?
This recall has been initiated to provide a labeling update with revised instruction how to operate the unit with Cold Therapy pads.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Gentherm Medical, LLC
Gentherm Medical, LLC has 2 total recalls tracked by RecallDetector.
Related Recalls
EndoVive Safety PEG Kit Recalled by Boston Scientific Corporation Due to Recall of kits which utilized ChloraPrep Triple Swabsticks...
Boston Scientific Corporation · February 10, 2026
Owner's Booklets and Instructions for Use that are used with Recalled by Trividia Health, Inc. Due to The system labeling (user manual and online labeling)...
Trividia Health, Inc. · February 6, 2026
Artelon FlexBand Dynamic Matrix Ref: 31057 Recalled by International Life Sciences Due to Augmentation devices failed bacterial endotoxin testing.
International Life Sciences · February 6, 2026
Owner's Booklets and Instructions for Use that are used with Recalled by Trividia Health, Inc. Due to The system labeling (user manual and online labeling)...
Trividia Health, Inc. · February 6, 2026
Owner's Booklets and Instructions for Use that are used with Recalled by Trividia Health, Inc. Due to The system labeling (user manual and online labeling)...
Trividia Health, Inc. · February 6, 2026
Data sourced from the FDA (Device). Last updated March 26, 2026. View original report