DRIVEMEDICAL RTLAGF-HP-STDRecalls & reported problems
Drive Devilbiss Healthcare · Personal CareHeating Pad Product Description: Moist Heating Pad,Std.Size, 1/ea,6/cs · Class 2
All models of DRIVEMEDICAL (111)
Data updated Oct 16, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 2
- Deaths reported
- 0
- Injuries reported
- 1
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 00822383511160), received between Mar 2, 2022 and Mar 2, 2022 — classified as 1 injury, 1 malfunction.
The most frequently reported specific device problem is “Overheating of Device” (1 report).
Reports come from manufacturers, hospitals and patients and are not verified by the FDA. A report does not prove the device caused the event, and counts can't be used to compare devices or estimate failure rates. What reports can and can't tell you · How this data works · Data updated Oct 16, 2026.
Most reported problems
Device problems
- Overheating of Device1
- Smoking1
- Temperature Problem1
Patient problems
- Burn(s)1
- No Clinical Signs, Symptoms or Conditions1
Recent adverse event reports
The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.
InjuryMar 2, 2022Temperature Problem; Temperature Problem
DRIVE DEVILBISS HEALTHCARE WAS NOTIFIED OF AN INCIDENT INVOLVING A HEATING PAD ON JANUARY 30TH. THE INITIAL REPORTER STATED THAT HER MOM "RECEIVED BURNS FROM A HEATING PAD" ON HER ARM AND " HAS BEEN IN PAIN FROM BLISTERING." THE UNIT HAS NOT BEEN RETURNED FOR EVALUATION AND NO ADDITIONAL INFORMATION IS AVAILABLE AT THIS TIME. DRIVE DEVILBISS HEALTHCARE IS CURRENTLY INVESTIGATING THE INCIDENT, INCLUDING ATTEMPTING TO RETRIEVE THE PRODUCT AND INSPECT IT, AND WILL FILE AN UPDATE AS SOON AS ADDITIONAL INFORMATION BECOMES AVAILABLE.
Patient problems: Burn(s)
MAUDE report 13656593 ↗MalfunctionMar 2, 2022Overheating of Device; Smoking; Overheating of Device; Smoking
ON (B)(6) 2022, DRIVE RECEIVED A MEDWATCH REPORT, RELATED TO A HEATING PAD. THE MEDWATCH REPORT WAS COMPLETED ON (B)(6) 2021. THE END USER REPORTED THAT "THE UNIT FELT LIKE IT WAS GETTING TOO HOT, SO I REMOVED IT. I THEN NOTICED THE UNIT SMOKING, SO I IMMEDIATELY UNPLUGGED IT AND THEN NOTICED BURN MARKS ON THE PLASTIC INNER COVER AND THE OTHER CLOTH COVER." DRIVE IS CURRENTLY INVESTIGATING THE INCIDENT, INCLUDING ATTEMPTING TO RETRIEVE THE PRODUCT AND INSPECT IT, AND WILL FILE AN UPDATE AS SOON AS ADDITIONAL INFORMATION BECOMES AVAILABLE.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 13654927 ↗
Other PAD, HEATING, POWERED devices
- HANDY SOLUTIONS HEATING PAD WRAP SHOULDER AND NECK 25607Navajo Manufacturing Company · Pad, Heating, Powered1 recall25 reports
- TearCare(TM) (2.2) System Kit FG 06041Sight Sciences, Inc. · Pad, Heating, Powered1 recall0 reports
- CHATTANOOGA 1032Djo, LLC · PAD, HEATING, POWERED6 reports
- DMI 619-5133-1900D-M-S Holdings, Inc. · Pad, Heating, Powered5 reports
- Sunbeam 053891133784Jarden Consumer Solutions · Pad, Heating, Powered5 reports
- Sunbeam 053891134019Jarden Consumer Solutions · Pad, Heating, Powered5 reports
- Sunbeam 053891174015Jarden Consumer Solutions · Pad, Heating, Powered4 reports
- CONAIR HP01XFConair Corporation · Pad, Heating, Powered3 reports
Sources and updates
- Device record: FDA GUDID, file dated Oct 13, 2026 · View this device in AccessGUDID ↗
- Adverse event reports: FDA MAUDE, file dated Oct 14, 2026 · each report above links to its original FDA record
- Recalls: FDA Medical Device Recalls, file dated Oct 16, 2026
- Page last rebuilt: Oct 16, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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