DMI 619-5133-1900Recalls & reported problems
D-M-S Holdings, Inc. · XL Electric Heating Pad · Class 2
Data updated Oct 16, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 5
- Deaths reported
- 0
- Injuries reported
- 5
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 5 adverse event reports that list this exact device (DI 00041298051336), received between Oct 17, 2024 and Apr 11, 2026 — classified as 5 injuries.
The most frequently reported specific device problem is “Improper or Incorrect Procedure or Method” (2 reports).
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.
Reports received per month
Most reported problems
Device problems
- Improper or Incorrect Procedure or Method2
- Adverse Event Without Identified Device or Use Problem1
- Excessive Heating1
- Overheating of Device1
- Unintended Electrical Shock1
Patient problems
- Burn(s)3
- Partial thickness (Second Degree) Burn2
- Blister1
- Electric Shock1
- Fluid Discharge1
- Pain1
- Skin Discoloration1
- Superficial (First Degree) Burn1
Recent adverse event reports
The 5 most recent of 5 reports, in the reporter's own words as published by the FDA.
InjuryApr 11, 2026Adverse Event Without Identified Device or Use Problem
CUSTOMER REPORTED HEATING PAD BURNT MY LEG.
Patient problems: Partial thickness (Second Degree) Burn; Superficial (First Degree) Burn
MAUDE report 24852197 ↗InjuryJan 7, 2026Unintended Electrical Shock
ITEM SHOCKED USER AND BURN MARK APPEARED.
Patient problems: Burn(s); Electric Shock
MAUDE report 23991465 ↗InjuryJul 22, 2025Overheating of Device; Overheating of Device
UNIT WAS HOT AND DID NOT SHUT OFF CORRECTLY CAUSING A BURN.
Patient problems: Burn(s)
MAUDE report 22569960 ↗InjuryJan 27, 2025Improper or Incorrect Procedure or Method; Excessive Heating; Improper or Incorrect Procedure or Method; Excessive Heating
CUSTOMER REPORTED USING HEATING PAD ON ELBOW AND AFTER 1 HOUR IT CAUSED A BURN ON BOTTOM OF ELBOW.
Patient problems: Burn(s); Skin Discoloration
MAUDE report 21240572 ↗InjuryOct 17, 2024Improper or Incorrect Procedure or Method; Improper or Incorrect Procedure or Method
DUE TO JOINT PAINT, PATIENT WENT TO BED WITH HEATING PAD ON ANKLE AND WORK UP 4 HOURS LATER TO PAIN. THE NEXT DAY PATIENT HAD SEVERE LEG PAIN AND THE SKIN WAS PEELING/BLISTERING. PATIENT WENT TO DOCTOR AND WAS TOLD PATIENT HAD 2ND DEGREE BURN.
Patient problems: Blister; Fluid Discharge; Pain; Partial thickness (Second Degree) Burn
MAUDE report 20471378 ↗
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
- 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
- CONAIR HP15XFConair 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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