MAUDE Adverse Event Report: Gentherm Medical, LLC Blanketrol

Model Number	233
Medical Device Problem Code	Overheating of Device (1437)
Health Effect - Clinical Code	No Clinical Signs, Symptoms or Conditions (4582)
Date of Event	06/29/2026
Type of Reportable Event	Malfunction
Event or Problem Description
The customer claims that the device has power to the switch but no display.
Additional Manufacturer Narrative
Complaint #(b)(4) received.This device was not returned however, the cpu board was returned and evaluated.Evidence of overheating was visually observed.

• Brand Name: Blanketrol
• Common Device Name: Blanketrol
• Manufacturer (Section D): Gentherm Medical, LLC; 12011 mosteller rd; cincinnati OH 45241
• Manufacturer (Section G): Gentherm Medical, LLC; 12011 mosteller rd; cincinnati OH 45241
• Manufacturer Contact: angie gegner ; 12011 mosteller rd; cincinnati, OH 45241 ; +1(513)326-5228
• MDR Report Key: 50057728
• Report Number: 1516825-2026-00019
• Device Sequence Number: 16124069
• Product Code: DWJ
• UDI-Device Identifier: 10613031861075
• UDI-Public: (01)10613031861075
• Combination Product (Y/N): N
• Initial Reporter State: KY
• Initial Reporter Country: US
• PMA/510(K) Number: k101589
• Number of Events Summarized: 1
• Summary Report (Y/N): N
• Reporter Type: Manufacturer
• Initial Reporter Occupation: Biomedical Engineer
• Type of Report: Initial
• Report Date (Section B): 07/28/2026

1 Device was Involved in the Event

1 Patient was Involved in the Event

• Is this an Adverse Event Report?: No
• Is this a Product Problem Report?: Yes
• Device Model Number: 233
• Device Catalogue Number: 86107
• Was Device Available for Evaluation?: No
• Is the Reporter a Health Professional?: No
• Type of Report(Section G): Thirty-Day
• Initial Date Received by Manufacturer: 09/19/2023
• Initial Report FDA Received Date: 07/28/2026
• Was Device Evaluated by Manufacturer? (Y/N): No
• Date Device Manufactured: 03/04/2022
• Is the Device Labeled for Single Use? (Y/N): No
• Is This a Single-Use Device that was Reprocessed and Reused on a Patient? (Y/N): No
• Usage of Device: Unknown
• Patient Sequence Number: 1
• Patient Sex: Unknown