MAUDE Adverse Event Report: NINGBO UNICO PRODUCTS CO., LTD HANDY SOLUTIONS; HEATING PAD WRAP SHOULDER /NECK

Model Number	25607 V1
Medical Device Problem Code	Temperature Problem (3022)
Health Effect - Clinical Code	Insufficient Information (4580)
Date of Event	03/30/2026
Type of Reportable Event	Serious Injury
Additional Manufacturer Narrative
The manufacturer received a report stating that the heating pad overheated, along with photos of the incident.The device was not returned for evaluation.The product label warned against use on soft surface and can't be covered during use, yet these actions were observed in the incident photos.Third-party testing confirmed the product does not overheat under correct use (see test report (b)(4)) and no defects identified.Third part testing report (b)(4).
Event or Problem Description
Patient using handy solution heating pad when it caught fire.Patient states it was only the 2nd use on a new heating pad.She states she smelled smoke/burning plastic before she heard the smoke detector or felt any pain due to her neuropathy.Member reports redness and pain on the skin in the area where the heating pad had been.She reports no blisters or deeper burns, she used aloe and the area healed in a few weeks.Patient has neuropathy potentially causingher not to feel the overheating of the heating pad before it caught fire.

• Brand Name: HANDY SOLUTIONS
• Common Device Name: HEATING PAD WRAP SHOULDER /NECK
• Manufacturer (Section D): NINGBO UNICO PRODUCTS CO., LTD ; no. 5 hongda rd, jiangbei, ; ningbo; ningbo, zhejiang 31500 0; CH 315000
• Manufacturer (Section G): NINGBO UNICO PRODUCTS CO., LTD ; no. 5 hongda rd, jiangbei,; ningbo; ningbo, zhejiang 31500 0; CH 315000
• Manufacturer Contact: alice fei ; no. 5 hongda rd, jiangbei, ningbo,zhejiang china. ; ningbo, zhejiang 31500-0 ; CH 315000
• MDR Report Key: 24949293
• Report Number: 3030539818-2026-00010
• Device Sequence Number: 10105766
• Product Code: IRT
• UDI-Device Identifier: 00024291256076
• UDI-Public: 024291256076
• Combination Product (Y/N): N
• Initial Reporter Country: US
• Number of Events Summarized: 1
• Summary Report (Y/N): N
• Serviced by Third Party (Y/N): Unknown
• Reporter Type: Manufacturer
• Report Source: Company Representative
• Initial Reporter Occupation: Pharmacist
• Type of Report: Initial
• Report Date (Section B): 03/30/2026

1 Device was Involved in the Event

1 Patient was Involved in the Event

• Is this an Adverse Event Report?: Yes
• Is this a Product Problem Report?: No
• Operator of Device: Lay User/Patient
• Device Model Number: 25607 V1
• Was Device Available for Evaluation?: No
• Is the Reporter a Health Professional?: Yes
• Type of Report(Section G): Initial
• Initial Date Received by Manufacturer: 04/06/2026
• Initial Report FDA Received Date: 04/22/2026
• Was Device Evaluated by Manufacturer? (Y/N): Yes
• Date Device Manufactured: 10/07/2024
• Is the Device Labeled for Single Use? (Y/N): No
• Is This a Single-Use Device that was Reprocessed and Reused on a Patient? (Y/N): No
• Usage of Device: Reuse
• Patient Sequence Number: 1
• Outcome Attributed to Adverse Event: Required Intervention
• Patient Age: 64 YR
• Patient Sex: Female
• Patient Weight: 70 KG
• Patient Ethnicity: Hispanic
• Patient Race: American Indian Or Alaskan Native