FDA Adverse Event
Injury
Summary report: N
OZINATING UVC GERMICIDAL LAMP
MDR report key: 10086833
·
Received May 22, 2020
Report
- Report Number
- MW5094667
- Event Type
- Injury
- Date Received
- May 22, 2020
- Date of Event
- April 21, 2020
- Report Date
- May 20, 2020
- Manufacturer
- UNK
- Product Code
- MKB
- Adverse Event
- Yes
- Product Problem
- Yes
- Report Source
- Voluntary report
- Reporter Location
- SC, US
- Reporter Occupation
- PATIENT
Narratives
Description of Event or Problem · 1
I HAVE VISION DAMAGE FROM OZONATING UVC LIGHT SIMILAR TO (B)(6) PRODUCT ALSO RESPIRATORY ISSUES. FDA SAFETY REPORT ID# (B)(4).
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 548078 | OZINATING UVC GERMICIDAL LAMP | DEVICE, GERMICIDAL, ULTRAVIOLET | MKB | UNK |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 | 36 YR | Required Intervention| S |