CONAIR HP15XFRecalls & reported problems
Conair Corporation · Heating Pad · Class 2
Data updated Oct 16, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 3
- Deaths reported
- 0
- Injuries reported
- 2
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 3 adverse event reports that list this exact device (DI 00074108355577), received between Aug 21, 2018 and Feb 26, 2019 — classified as 2 injuries, 1 malfunction.
The most frequently reported specific device problem is “Device Emits Odor” (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
- Device Emits Odor1
- Fire1
- Inappropriate/Inadequate Shock/Stimulation1
Patient problems
- Electric Shock1
- No Consequences Or Impact To Patient1
- No Known Impact Or Consequence To Patient1
Recent adverse event reports
The 3 most recent of 3 reports, in the reporter's own words as published by the FDA.
MalfunctionFeb 26, 2019Fire
ON 1/28/2019 - THE CONSUMER CLAIMS THE PRODUCT CAUGHT ON FIRE. THE CONSUMER HUNG UP ON OUR CALL CENTER PRIOR GIVING A FULL DESCRIPTION.
Patient problems: No Known Impact Or Consequence To Patient
MAUDE report 8370046 ↗InjuryDec 18, 2018Inappropriate/Inadequate Shock/Stimulation
ON (B)(6) 2018 THE CONSUMER CLAIMS TO HAVE RECEIVED A SHOCK WHILE IN USER OF THE PRODUCT. THE CONSUMER STATES THAT THE PRODUCT IS RIPPED A LITTLE BECAUSE OF THE USE. THE CONSUMER DISCARDED THE PRODUCT AND HAS AGREED TO RECEIVE A REPLACEMENT.
Patient problems: Electric Shock
MAUDE report 8173552 ↗InjuryAug 21, 2018Device Emits Odor
ON (B)(6) 2018 - THE CONSUMER CLAIM WAS USING THE PRODUCT IN THE CHIN AREA FOR A TOOTHACHE AND BEGAN TO DOZE OFF. AWOKE TO SMELL OF SMOKE AND UNPLUGGED THE HEATING PAD. THREW IT OUTSIDE DUE TO STRONG SMELL. THERE WAS NO DAMAGE TO PROPERTY AND NO PERSONAL INJURY. SHE WOULD LIKE THE HEATING PAD REPLACED.
Patient problems: No Consequences Or Impact To Patient
MAUDE report 7800755 ↗
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- 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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