Severity
Critical
CriticalClass IOngoing
FDA Devices recall · Reported April 1, 2026
Handy Solutions Neck & Shoulders Heating Pad, Number: 25607, Manufactured by Ninbo Unico Products Co., Ltd
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 …
Navajo Manufacturing Company recalled Handy Solutions Neck & Shoulders Heating Pad, Number: 25607, Manufactured by Ninbo Unico … - a critical-severity action.
Handy Solutions Neck & Shoulders Heating Pad, Number: 25607, Manufactured by Ninbo Unico … was recalled by Navajo Manufacturing Company in April 1, 2026. Reason: If heating pad is folded while in use, the power density increases in the folded area causing excessive tempe…. Check the official notice for the remedy. Verify recall #Z-1588-2026 with the FDA Devices before acting.
The recall
Navajo Manufacturing Company issued this critical-severity FDA Devices recall-If heating pad is folded while in use, the power density increases in the folded area causing excessive tempe….
- Critical
- severity level
- 28K units
- affected scope
- Class I
- classification
- April 1, 2026
- reported
Sourced from official FDA Devices enforcement records. Verify recall #Z-1588-2026 with the agency before acting. Full product description, hazard, remedy, and related recalls are below.
Recall Insight
This FDA Devices action (record #Z-1588-2026) was formally reported on April 1, 2026, with the manufacturer initiating the action on February 18, 2026. It is classified under Critical severity (Class I), with a current status of Ongoing. Navajo Manufacturing Company is listed as the recalling firm, operating out of Denver, CO. Federal records list the affected scope as 28,457.
The documented reason for this recall is: 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… Distribution data in the federal record shows the product reached: US Nationwide distribution in the states of CA, MS, FL, IN, LA, VA, TX.. Distribution scope directly affects the consumer exposure window and determines whether a recall remains regional or escalates into a nationwide advisory.
Within the same product category the archive holds 6 closely related recalls, 3 from FDA Devices - clustering in a narrow category often points to a systemic quality-control or supplier issue rather than a one-off defect. Always verify the recall number against the official agency record before acting.
Medical Devices recalls over time
Where this recall sits in its category - 40,322 medical devices recalls on record
Of 101,704 recalls in the database, 24,878 are high severity, 72,426 moderate, and 4,400 low. This recall is classified high severity.
Counts reflect market size and reporting activity, not inherent danger, we do not rank products by risk from raw recall volume.
Affected scope
28,457
Related Recalls
6
3 from same agency
Product description
Handy Solutions Neck & Shoulders Heating Pad, Number: 25607, Manufactured by Ninbo Unico Products Co., Ltd
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.
Recall Profile
| Attribute | Value |
|---|---|
| Agency | U.S. Food and Drug Administration |
| Severity class | Critical (Class I) |
| Status | Ongoing |
| Recall number | Z-1588-2026 |
| Date reported | April 1, 2026 |
| Date initiated | February 18, 2026 |
| Recalling firm | Navajo Manufacturing Company |
| Firm location | Denver, CO |
| Affected scope | 28,457 |
| Distribution | US Nationwide distribution in the states of CA, MS, FL, IN, LA, VA, TX. |
Profile values are sourced directly from the official FDA Devices enforcement record. Source: U.S. Food and Drug Administration.
What to do with this recall
Match your product against the recall record, then act on the agency remedy.
- Check the recall number (Z-1588-2026) and product description against the item you own. Search the archive
- Confirm the current status with FDA Devices before acting, recall details can be updated.
- This is a Class I (high-risk) recall, stop using the product immediately and follow the disposal or return instructions. What to do next
This page summarizes the official FDA Devices record for research and awareness; it is not legal, medical, or safety advice. Verify with the issuing agency before acting.
Frequently Asked Questions
What product was recalled? ▼
Handy Solutions Neck & Shoulders Heating Pad, Number: 25607, Manufactured by Ninbo Unico Products Co., Ltd. Recalled by Navajo Manufacturing Company. Units affected: 28,457.
Why was this product recalled? ▼
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.
Which agency issued this recall? ▼
This recall was issued by the FDA Devices on April 1, 2026. Severity: Critical. Recall number: Z-1588-2026.
Where was the recalled product distributed? ▼
Distribution: US Nationwide distribution in the states of CA, MS, FL, IN, LA, VA, TX..
How do I check if my product is affected by a recall? ▼
Check the product description and recall number (Z-1588-2026) against your product. Visit the official FDA Devices website for the most current information. You can also use our Recall Checker tool to search by product name or brand.
Should I stop using a recalled medication or medical device? ▼
Do not stop using a recalled medication or device without consulting your healthcare provider first, as abruptly discontinuing treatment could pose its own health risks. Your doctor can advise on alternatives or whether the recall applies to your specific product lot. Check the recall number and lot information against your product packaging.
Nearby Recalls in This Category
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Every figure on PlainRecalls is rendered directly from official FDA, CPSC and NHTSA recall records, no number is typed in by an editor. This recall: FDA Devices, reported April 1, 2026. Severity classes follow each agency's own taxonomy (FDA Class I/II/III; CPSC and NHTSA by hazard type), and related-recall context is computed across the full archive. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error. Data current as of July 2026.