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