| Brand Name | HANDY SOLUTIONS NECK AND SHOULDERS HEATING PAD |
| Common Device Name | PAD, HEATING, POWERED |
| Manufacturer (Section D) |
| NINGBO UNICO PRODUCTS CO., LTD |
| floor.3th, building 5, no.5 |
| hongda rd |
| jiangbei, ningbo zhejiang 31503 3 |
| CH 315033 |
|
| MDR Report Key | 24667905 |
| Report Number | 1000065475-2026-00006 |
| Device Sequence Number | 21143246 |
| Product Code |
IRT
|
| UDI-Device Identifier | 00024291256076 |
| UDI-Public | 00024291256076 |
| 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) | N |
| Reporter Type |
Importer
|
| Initial Reporter Occupation |
Pharmacist
|
| Type of Report
| Initial |
| Report Date (Section B) |
02/25/2026 |
| Report Date (Section F) |
03/23/2026 |
| 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 |
| Was Device Available for Evaluation? |
No
|
| Is the Reporter a Health Professional? |
Yes
|
| Was the Report Sent to FDA? |
Yes
|
| Distributor Facility Aware Date | 02/25/2026 |
| Device Age | 1 YR |
| Event Location |
Home
|
| Date Report to Manufacturer | 02/26/2026 |
| Initial Date Received by Manufacturer | Not provided |
| Initial Report FDA Received Date | 03/23/2026 |
Is This a Single-Use Device that was Reprocessed and Reused on a Patient? (Y/N) |
No
|
| Patient Sequence Number | 1 |
| Outcome Attributed to Adverse Event |
Other;
|
| Patient Sex | Unknown |
| Date Report Sent to FDA | 03/23/2026 |
|
|