FDA Adverse Event
Malfunction
Summary report: N
PHILLIPS
MDR report key: 23881373
·
Received December 23, 2025
Report
- Report Number
- MW5181096
- Event Type
- Malfunction
- Date Received
- December 23, 2025
- Report Date
- December 17, 2025
- Manufacturer
- PHILLIPS / PHILIPS ULTRASOUND LLC
- Product Code
- IYN
- Product Problem
- Yes
- Report Source
- Voluntary report
- Reporter Location
- SC, US
- Reporter Occupation
- OTHER HEALTH CARE PROFESSIONAL
- Health Professional
- Yes
Narratives
Description of Event or Problem · 0
PHILLIPS LUMIFY ULTRASOUND DEVICE UNABLE TO KEEP A CHARGE AND NOT ABLE TO USE.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 1647319 | PHILLIPS | SYSTEM, IMAGING, PULSED DOPPLER, ULTRASONIC | IYN | PHILLIPS / PHILIPS ULTRASOUND LLC |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 | NA | Unknown |