FDA recall, , High risk
Handy Solutions Neck & Shoulders Heating Pad
The heating pad can cause burns to persons and property if folded or placed under the body.
Summary by Recall Canary from the FDA notice
What happened
Navajo Manufacturing Company of Denver, Colorado, recalled the Handy Solutions Neck & Shoulders Heating Pad, Number 25607, manufactured by Ninbo Unico Products Co., Ltd, because if the heating pad is folded while in use, the power density increases in the folded area causing excessive temperatures, which can also be caused by placing the pad under the body, and then the high limit device is unable to sense the higher temperature so power is not terminated.
This may cause a burning smell prior to melting or burning, potentially causing burns to persons and property.
The company began the recall on February 18, 2026, and the FDA classified it on March 20, 2026. The product was distributed nationwide in the states of California, Florida, Indiana, Louisiana, Mississippi, Texas and Virginia.
What to do
We don't have product-specific instructions for this recall. FDA's general advice for medical device recalls:
- A device recall doesn't always mean you must stop using it: it may need to be checked, adjusted or fixed.
- Talk to your health care provider before you stop using it.
Is yours affected?
Affected if its UDI-DI matches.
A UDI-DI is the device identifier printed with the barcode on the device label.
Handy Solutions Neck & Shoulders Heating Pad, Number: 25607, Manufactured by Ninbo Unico Products Co., Ltd
- UDI-DI
- 00024291256076
Recall details
- Company began the recall
- Sold in
US Nationwide distribution in the states of California, Mississippi, Florida, Indiana, Louisiana, Virginia, Texas.
- Company
- Navajo Manufacturing CompanyDenver, Colorado
- Hazard
- Device defect
- Risk
High risk
There is a reasonable chance that using it could cause serious health problems or death.
FDA Class I recall · How risk is rated
- Event ID
- 98453
- Recall number
- Z-1588-2026
Timeline
FDA's Enforcement Report is its public list of recalls; FDA adds a recall when it posts it and publishes the list weekly.
Company began the recall
Classified by FDA
Added to FDA's Enforcement Report
In FDA's weekly enforcement report
Listed on Recall Canary
Summary updated
