---
title: "Handy Solutions Neck & Shoulders Heating Pad, Number: 25607, Manufactured by ... — FDA record Z-1588-2026 | Is It on Recall"
description: "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 un"
url: https://isitonrecall.com/recall/fda-device-z-1588-2026-handy-solutions-neck-shoulders-heating-pad-number-25607-manufactured-by-ninbo-unico-products-co-ltd/
updated: 2026-10-01
site: "Is It on Recall"
language: en
---

[Recall archive](https://isitonrecall.com/archives/) / FDA device enforcement

# Handy Solutions Neck & Shoulders Heating Pad, Number: 25607, Manufactured by Ninbo Unico Products Co., Ltd — FDA record Z-1588-2026

Reported ongoing

Status as reported in the agency record. FDA warns that enforcement status may not track the current recall lifecycle; check the current official notice.

Source date Feb 18, 2026. Retrieved Oct 1, 2026. Last updated Oct 1, 2026.

Archive changed Oct 1, 2026. USDA FSIS records are unavailable; [check FSIS directly](https://www.fsis.usda.gov/recalls). [Source coverage and dates](https://isitonrecall.com/sources/).

## What the record says

- **Product**: Handy Solutions Neck & Shoulders Heating Pad, Number: 25607, Manufactured by Ninbo Unico Products Co., Ltd
- **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 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.
- **Classification**: Class I
- **Recalling firm**: Navajo Manufacturing Company
- **Quantity**: 28,457
- **Agency-reported status**: Ongoing
- **Source record identifier**: Z-1588-2026

[Open the official record](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1588-2026%22)

[What the recall classes mean](https://isitonrecall.com/guides/recall-classes/). Classification is an agency assessment, not individual medical advice.

## Lot and product identifiers

| Label field | Details supplied by the agency |
| --- | --- |
| Lot, code or applicability | UPC: 0-24291-25607-6, UDI-DI: 00024291256076 |

Match all identifying details in the current notice. A brand name alone is not enough.

## Distribution

US Nationwide distribution in the states of CA, MS, FL, IN, LA, VA, TX.

States below are derived from the distribution text, including nationwide wording. They are not inferred from the firm's address.

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- [Oregon](https://isitonrecall.com/state/oregon/)
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- [Utah](https://isitonrecall.com/state/utah/)
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- [Wyoming](https://isitonrecall.com/state/wyoming/)

## Dates in the source

- **Report date**: Apr 1, 2026
- **Recall initiation date**: Feb 18, 2026
- **Center classification date**: Mar 20, 2026

FDA company pages use the listing date; enforcement records use initiation dates; CPSC uses recall date; NHTSA uses report-received date. These dates are not interchangeable.

## What to do next

Read the official notice for the action that applies to your exact product.

[Read the current instructions](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1588-2026%22)

## Related records

[Medical devices records](https://isitonrecall.com/category/medical-devices/) [Navajo Manufacturing Company records](https://isitonrecall.com/brand/navajo-manufacturing-company/)
