FDA Adverse Event
Injury
Summary report: N
PKR
MDR report key: 6260937
·
Received January 17, 2017
Report
- Report Number
- MW5067305
- Event Type
- Injury
- Date Received
- January 17, 2017
- Date of Event
- May 13, 2015
- Report Date
- January 17, 2017
- Product Code
- HLQ
- Adverse Event
- Yes
- Report Source
- Voluntary report
- Reporter Location
- CO, US
- Reporter Occupation
- PATIENT
Narratives
Description of Event or Problem · 1
THE AMOUNT OF FLOATERS IN THE EYE HAS INCREASED AFTER GETTING PKR ON EYES. I WASN'T A CANDIDATE FOR LASIK BECAUSE MY LINING WAS TOO THIN. LASIK VISION INSTITUTE.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 41327 | PKR | PKR | HLQ |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 | 38 YR | Disability |