FDA Adverse Event Injury Summary report: N

BAUSCH & LOMB MOISTURE LOC

MDR report key: 855189 · Received May 19, 2007

Report

Report Number
MW5001939
Event Type
Injury
Date Received
May 19, 2007
Date of Event
June 28, 2005
Report Date
May 19, 2007
Manufacturer
BAUSCH & LOMB RENU MOISTURE LOC
Product Code
LPN
Product Problem
Yes
Report Source
Voluntary report
Reporter Location
AL, US

Narratives

Description of Event or Problem · 1

I WAS USING BAUSCH & LOMB MOISTURE LOC AND HAD AN EYE IRRITATION; I WENT TO THE DOCTOR IN 2005. I WAS TOLD BY THE DOCTOR NOT TO WEAR CONTACT LENS FOR A WHILE BECAUSE I HAD AN INFECTION IN MY EYE. SHE TOLD ME TO MAKE SURE THE IRRITATION HAD CLEARED UP BEFORE I WEAR CONTACTS AGAIN. THE DOCTOR THEN PRESCRIBED A PRESCRIPTION FOR EYE GLASSES. I WORE THESE EYE GLASSES FOR 8 TO 10 MONTHS. AFTER THAT MY EYES WERE BETTER. I HAVE REPORTED THIS CASE. I WAS PRESCRIBED PRESCRIPTION EYE GLASSES. MY RECORDS HAS BEEN GIVEN TO THE ATTORNEYS.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 BAUSCH & LOMB MOISTURE LOC BAUSCH & LOMB LPN BAUSCH & LOMB RENU MOISTURE LOC

Patients

Seq Age Sex Outcome Treatment
1 40 YR Disability