U.S. Food and Drug Administration - CDRH Mobile
Skip NavigationFDA Logo links to FDA home pageCenter for Devices and Radiological Health, U.S. Food and Drug AdministrationHHS Logo links to Department of Health and Human Services website
FDA Home Page | CDRH Home Page | Search | A-Z Index U.S. Food and Drug AdministrationCenter for Devices and Radiological Health Questions?
horizonal rule
Medical Device Safety: FDA's Resource for Health Care Professionals On Device Recalls, Alerts, and Other Safety Information
Home
Search
Alerts
Recalls
Tips & Articles
Report a Problem
Adverse Events Database
FDA Patient Safety News Webcasts
SubscribeSubscribe to Email Updates on Medical Device Safety

Advice for Patients: Possible Burns or Fires from Heating Pads Manufactured by HoMedics, Inc.

Issued: July 11, 2007

Background

On February 9, 2007, HoMedics, Inc. recalled their TheraP model heating pads after receiving complaints from users that these products had caused fires and burns. For a complete list of the recalled pads, see below.

The source of the problem may be a loose connection in the heating pad which could cause a short circuit. This may pose a risk of burns, fire, and damage to materials in close contact to the heating pad, such as bedding, furniture, or clothing.

The voluntary recall includes approximately 292,108 heating pads produced in 2001 and shipped to retailers in 2001 and 2002. These heating pads were sold in the U.S. to Walgreens and other retail drug and department stores.

illustration, back view of hand control. Disregard 9 digit number; note the 4-digit date code only (example pictured is 1901). Any 4 digit code ending in 01 is subject to this recall. Numbers ending in 02, 03, 04, 05, and 06 are not subject to this recallAdvice for Patients

  • Check the models below to see if you have one of the affected heating pads:
    • Walgreen’s by Homedics® Model 802857 Standard Size Moist/Dry Heating Pad
    • HoMedics® Thera-P® Model HP-100 Standard Size Dry Heating Pad
    • HoMedics® Thera-P® Model HP-150 Standard Size Moist/Dry Heating Pad
    • HoMedics® Thera-P® Model HP-200 Standard Size Moist/Dry Heating Pad with Auto Shut-off
    • HoMedics® Thera-P® Model HP-300 King Size Moist/Dry Heating Pad
    • HoMedics® Thera-P® Model HP-500 King Size Moist/Dry Heating Pad with Auto Shut-off

Each HoMedics® heating pad is marked with a unique 4-digit date code located both on the back of the hand control as well as on the bottom panel of the packaging. ONLY 4-DIGIT DATE CODES ENDING IN "01" ARE SUBJECT TO THIS VOLUNTARY RECALL.

  • If you have one of the recalled pads, stop using it immediately and return it to the retailer for a full refund.
     
  • Report to the FDA's MedWatch Adverse Event Reporting program (see below).

For More Information about the Homedics Heating Pad recall, check:

For more about general heating pad safety, check:

  • The FDA/CPSC Public Health Advisory: Hazards Associated with the Use of Electric Heating Pads at http://www.fda.gov/cdrh/heatpad.pdf. Although this Advisory was released in 1995, the recommendations are still valid.

Consumers with questions may contact:

  • HoMedics, Inc . at 1-800-466-3342, John Wettlaufer at 1-249-863-3000 ext. 1168, or email cservice@homedics.com.

MedWatch Reporting

Consumers who have experienced adverse reactions or quality problems with the use of this product are also encouraged to report to the FDA's MedWatch Adverse Event Reporting program either online, by regular mail or by FAX.

 

Daniel G. Schultz, MD
Director
Center for Devices and Radiological Health
Food and Drug Administration

Updated July 25, 2007

horizonal rule

CDRH Home Page | CDRH A-Z Index | Contact CDRH | Accessibility | Disclaimer
FDA Home Page | Search FDA Site | FDA A-Z Index | Contact FDA | HHS Home Page

Center for Devices and Radiological Health / CDRH