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U.S. Department of Health and Human Services

MAUDE Adverse Event Report: HOLLYWOOD LUXURY CONTACT LENSES; LENSES, SOFT CONTACT, DAILY WEAR
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HOLLYWOOD LUXURY CONTACT LENSES; LENSES, SOFT CONTACT, DAILY WEAR Back to Search Results
Device Problem Patient-Device Incompatibility (2682)
Patient Problems Inflammation (1932); Pain (1994); Loss of Vision (2139); Eye Burn (2523)
Event Date 07/24/2021
Event Type  Injury  
Event Description
I went into a new gas station by my home and saw an entire row of non prescribed contact lenses for only (b)(6) and me being naive, i bought a pair.I debated using them but all the videos i watched indicated that it was safe.So i did.After about 1-2 minutes of wearing them my eyes began to burn and puff up.I immediately took them out.I made sure my hands were clean and my contacts were in the saline given by the gas station, so this pain was by no fault of my own, a day later i can't see anything at all and may be going blind from whatever was in that saline.Today i find out after doing some research that it's illegal to sell non prescription contact lenses especially at a gas station!!! so, these owners are preying on poor folk who are vulnerable and don't know any better, just to make a couple extra bucks!! they are selling illegal contacts that are taking away peoples eyesight for gods sake.All for greed.These people don't deserve to make money off of me going blind (ps i have photo proof but they will not upload and i'm not canceling this just because they won't upload).(b)(6) on (b)(6).
 
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Brand Name
HOLLYWOOD LUXURY CONTACT LENSES
Type of Device
LENSES, SOFT CONTACT, DAILY WEAR
MDR Report Key12318390
MDR Text Key266667077
Report NumberMW5103227
Device Sequence Number1
Product Code LPL
Number of Events Reported1
Summary Report (Y/N)N
Report Source Voluntary
Reporter Occupation Patient
Type of Report Initial
Report Date 08/11/2021
1 Device was Involved in the Event
1 Patient was Involved in the Event
Date FDA Received08/12/2021
Is this an Adverse Event Report? Yes
Is this a Product Problem Report? No
Device Operator No Information
Was Device Evaluated by Manufacturer? No Information
Type of Device Usage N
Patient Sequence Number1
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