Handy Solutions Neck & Shoulders Heating Pad, Number: 25607, Manufactured by Ninbo Unico Products Co., Ltd
Summary
The FDA issued a Class I for Handy Solutions Neck & Shoulders Heating Pad, Number: 25607, Manufactured by Nin by Navajo Manufacturing Company. Reason: If heating pad is folded while in use, the power density increases in the folded area causing excessive temperatures, which can also be caused by plac.
Details
Source
Device Recall
External ID
Z-1588-2026
Action Date
2026-04-01
Status
Ongoing
Category
device
Product Description
Handy Solutions Neck & Shoulders Heating Pad, Number: 25607, Manufactured by Ninbo Unico Products Co., Ltd
Lot/Code Info: UPC: 0-24291-25607-6, UDI-DI: 00024291256076
Quantity Affected: 28,457
Reason for Recall
If 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 pad under the body, then the high limit device is unable to sense the higher temperature so power is not terminated. May cause a burning smell prior to melting/burning potentially causing burns to persons and property.
Distribution
US Nationwide distribution in the states of CA, MS, FL, IN, LA, VA, TX.
Type: Voluntary: Firm initiated
Recall Initiated: 2026-02-18
Company
Denver, CO
Context & Analysis
This is a Class I recall. Class I recalls are the most serious — there is a reasonable probability that use of or exposure to the product will cause serious health consequences or death.
This was one of 161 device recalls issued in the same week, part of 403 device-related FDA actions this month.
Frequently Asked Questions
What is a Class I recall?
A Class I recall is the most serious type. The FDA has determined there is a reasonable probability that the product will cause serious adverse health consequences or death. Consumers should stop using the product immediately.
What should I do if I have this product?
Stop using the product. Check the product against the specific lot numbers or identifiers listed in the recall. Contact the manufacturer (Navajo Manufacturing Company) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does Navajo Manufacturing Company have FDA actions?
This is the only FDA action we have on record for Navajo Manufacturing Company in our database.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "Z-1588-2026" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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