Navajo Manufacturing Company recalls Handy Solutions Neck & Shoulders Heating Pad

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.

On 2/18/2026 a recall notice was emailed to one customer who was asked to do the following: Begin processes for notifying your distributors/customers who were shipped affected devices. They should return all unsold units to the recalling firm. Your customers should begin to notify their customers as well to discontinue use of the product. A Consumer Recall Notice will be included as a separate file that can be provided to the consumer. Retailers should notify consumers who received the recalled heating pad to immediately discontinue use of the heating pad, cut the heating pad s cord, and dispose of the heating pad. Consumers should immediately discontinue use of the heating pad. The heating pad's cord should be cut and the heating pad disposed of. The consumer will be contacted by the platform through which they purchased the heating pads to arrange replacement from a different manufacturer. Complete and return the Acknowledgement and Receipt Form to fmorales@navajoinc.com If you have questions, firm can be contacted via phone: 1-800-525-5097, or email: heatingpadrecall@navajoinc.com

• FDA enforcement recordOfficial FDA database entry for Z-1588-2026
• FDA device classification · IRTOfficial FDA classification for this device type
• CFR regulation · 21 CFR 890.5740The federal regulation governing this device
• FDA recall announcementSearch FDA.gov for the official press announcement
• Find Navajo Manufacturing CompanySearch for the manufacturer's official notice
• News coverageRecent reporting on this recall and manufacturer
• openFDA data recordThe raw JSON record this page is built from

Source: U.S. FDA openFDA device enforcement reports. This summary is informational and may lag or differ from the official record. Always verify against the FDA before acting.