Devices › Pad, heating, powered
Device brand name · Heating pad
Sunbeam: medical device reports filed with FDA
1,502 reports name it, 1999–2026. Manufacturer given most often on reports: Sunbeam Products. Product code IRT.
- 1,502
- device reports naming the brand
- 0% of all MAUDE reports · about 55 a year
- 29
- reports, 12 months to August 2026
- 46 in the 12 months before
- 55%
- classified as malfunction
- 70.1% across the product code
- 0.4%
- classified as death, as reported
- 6 reports · not verified by FDA
1,502 medical device reports received by FDA name the brand "Sunbeam" (heating pad); the manufacturer given most often on reports is Sunbeam Products; received from June 1999 to August 2026. Brand names are as the reporter or manufacturer wrote them, so one product can appear under several spellings.
29 reports arrived in the 12 months to August 2026, down 37% from 46 in the 12 months before. FDA releases MAUDE data monthly; reports can arrive months after an event, so the newest months grow in later releases. The event types recorded are malfunction (55%), injury (42.8%) and other (0.7%); across all pad, heating, powered reports (product code IRT) death is recorded in 0.2% and malfunction in 70.1%. Event type is the reporter's classification of the report, not a verified outcome.
The device problems coded most often are fire (28.3%), improper or incorrect procedure or method (13.6%) and labelling, instructions for use or training problem (12%). The patient problems coded most often are burn(s), burn, thermal and partial thickness (second degree) burn. FDA states that "MDR data alone cannot be used to establish rates of events, evaluate a change in event rates over time or compare event rates between devices. The number of reports cannot be interpreted or used in isolation to reach conclusions about the existence, severity, or frequency of problems associated with devices." It adds that the reporting system "has limitations, including the potential submission of incomplete, inaccurate, untimely, unverified, or biased data."
Reports by month, five years
Reports by the month FDA received them. FDA releases MAUDE data monthly; reports can arrive months after an event, so the newest months grow in later releases.
By year received
Event type and report source
Event type, as classified on the report
Who filed the report
Grey bar: all 6,882 reports carrying product code IRT. Event type is the filer's classification and is not verified by FDA.
Device problems coded
| Device problem (FDA code) | Reports | Share | Share across product code |
|---|---|---|---|
| Fire | 425 | 28.3% | 8% |
| Improper or incorrect procedure or method | 204 | 13.6% | 7.9% |
| Labelling, instructions for use or training problem | 180 | 12% | 2.5% |
| Thermal decomposition of device | 147 | 9.8% | 15.6% |
| Melted | 119 | 7.9% | 2.2% |
| Smoking | 104 | 6.9% | 5.1% |
| Overheating of device | 102 | 6.8% | 4.2% |
| Insufficient device problem information | 90 | 6% | 4.4% |
| Hole in material | 78 | 5.2% | 1.7% |
| Breakthe device broke | 46 | 3.1% | 2.9% |
| Collapse | 44 | 2.9% | 0.6% |
| Folded | 38 | 2.5% | 0.8% |
| Sticking | 35 | 2.3% | 0.6% |
| Device emits odor | 33 | 2.2% | 2.4% |
| Material discolored | 32 | 2.1% | 0.9% |
| Sparking | 28 | 1.9% | 27.9% |
| Device operates differently than expectedthe device behaved unexpectedly | 22 | 1.5% | 1.5% |
| Temperature problem | 17 | 1.1% | 1.2% |
| Failure to shut off | 14 | 0.9% | 1.3% |
| Wire(s), breakage of | 12 | 0.8% | 1.9% |
FDA's device problem codes as entered on the report; one report can carry several. Generic codes such as "no apparent adverse event" are left out.
Patient problems coded
| Patient problem (FDA code) | Reports | Share |
|---|---|---|
| Burn(s)a burn | 560 | 37.3% |
| Burn, thermal | 55 | 3.7% |
| Partial thickness (second degree) burn | 46 | 3.1% |
| Full thickness (third degree) burn | 40 | 2.7% |
| Injurya physical injury | 17 | 1.1% |
| Surgical procedure | 8 | 0.5% |
| Deaththe patient died; cause not stated by this term | 5 | 0.3% |
| Hospitalization required | 5 | 0.3% |
| Painpain, site not specified | 5 | 0.3% |
| Superficial (first degree) burn | 5 | 0.3% |
| Burning sensationa burning feeling | 4 | 0.3% |
| Complaint, ill-defined | 4 | 0.3% |
| Scarring | 4 | 0.3% |
| Swellingswelling | 4 | 0.3% |
| Blister(s) | 3 | 0.2% |
Patient problem codes are present mainly in reports filed since 2019 and are often blank.
In context
| Measure | Sunbeam | Product code IRT | All MAUDE reports |
|---|---|---|---|
| Reports | 1,502 | 6,882 | 26,136,888 |
| Share of that pool | — | 21.8% | 0% |
| Classified as death, per 1,000 reports | 4 | 2 | 9 |
| Classified as injury | 42.8% | 21% | 36.2% |
| Classified as malfunction | 55% | 70.1% | 62.3% |
| Filed by the manufacturer | 99.1% | 91.2% | 94.9% |
Shares are of reports, not of devices in use. FDA states that "MDR data alone cannot be used to establish rates of events, evaluate a change in event rates over time or compare event rates between devices. The number of reports cannot be interpreted or used in isolation to reach conclusions about the existence, severity, or frequency of problems associated with devices." It adds that the reporting system "has limitations, including the potential submission of incomplete, inaccurate, untimely, unverified, or biased data."
Other brands with product code IRT
| Brand | Reports | Latest 12 months | Classified as death |
|---|---|---|---|
| Thermophore | 1,970 | 0 | 0.1% |
| Thermophore Automatic Moist Heat Pack | 1,321 | 0 | 0% |
| Thermophore Automatic Heat Pack | 305 | 0 | 0% |
| Thermophore Arthritis Pad | 272 | 0 | 0% |
| Mighty Bliss | 250 | 0 | 0% |
| Softheat | 251 | 0 | 0.4% |
| Conair | 312 | 10 | 0% |
| Conmed | 900 | 89 | 0.2% |
Ordered by report count for navigation only. FDA states that "MDR data alone cannot be used to establish rates of events, evaluate a change in event rates over time or compare event rates between devices. The number of reports cannot be interpreted or used in isolation to reach conclusions about the existence, severity, or frequency of problems associated with devices." It adds that the reporting system "has limitations, including the potential submission of incomplete, inaccurate, untimely, unverified, or biased data." FDA also states that "common products may have a higher number of adverse events due to the higher total number of people using the product."
Questions about Sunbeam reports
How many FDA reports name Sunbeam?
1,502 medical device reports in the openFDA MAUDE release of 28 Sep 2026, covering reports received through August 2026; 29 in the latest 12 months.
What kinds of events are reported?
malfunction (55%), injury (42.8%) and other (0.7%). "Event type" is how the report was classified when filed: death, injury, malfunction or other.
What device problems are coded?
fire (28.3%), improper or incorrect procedure or method (13.6%), labelling, instructions for use or training problem (12%), thermal decomposition of device (9.8%) and melted (7.9%). These are FDA's device problem codes as entered on the report.
Who files these reports?
manufacturer reports (99.1%), voluntary reports (0.9%) and distributor reports (0.1%). Manufacturers and user facilities are required to report; voluntary reports come from health professionals and the public.
Do these reports show that Sunbeam was at fault?
No. FDA states that "MDR data alone cannot be used to establish rates of events, evaluate a change in event rates over time or compare event rates between devices. The number of reports cannot be interpreted or used in isolation to reach conclusions about the existence, severity, or frequency of problems associated with devices." It adds that the reporting system "has limitations, including the potential submission of incomplete, inaccurate, untimely, unverified, or biased data." FDA adds that "a causal relationship cannot be established between product and reactions listed in a report."
How do I report a problem with a medical device?
Through FDA MedWatch (Form FDA 3500 for health professionals and consumers), or to the manufacturer. See the guide on how to report.
Where this comes from. Counts are built from the openFDA Device Adverse Event (MAUDE) bulk export released 28 Sep 2026, which holds reports FDA received through 31 Aug 2026. Brand, generic and manufacturer names are as written on the reports; product code names come from FDA's device classification. A report counts here when any device it lists carries this brand name after punctuation and capitalisation are normalised. No report narrative, lot number, patient detail or reporter identity is published. See the methodology and sources; FDA's record is authoritative, and corrections are handled within five working days.
Drug data (FAERS) through 30 Jun 2026; device data (MAUDE) through 31 Aug 2026. Not medical advice.