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U.S. Department of Health and Human Services

MAUDE Adverse Event Report: CLEAR EYE
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CLEAR EYE Back to Search Results
Device Problem Insufficient Information (3190)
Patient Problems Conjunctivitis (1784); Blurred Vision (2137); Burning Sensation (2146)
Event Type  Other  
Event Description
Good afternoon, i am a beautiful black woman and i wanted to have honey eyes to go with my beauty.I went for an eye exam in the later part of 2016 and got the exam and order my contacts.I wore the contacts one week and got pink eye in my left eye.Went to the doctor and got drops.When the pink eye cleared, i went back to the contacts and noticed that when i used the solution, my left eye was burning and vision blurrier.I went back and the doctor told me to stop wearing the contacts and put some drops in my eye and come back in 2 weeks.I was fine until this morning and i put my right eye in and it burn something awful once i got it calmed down.I went to work and now both eyes are very blurry and it's almost impossible to function.I realized that it is the solutions and i pray that i don't mess my vision completely up.I will never buy this product again and tell all my family and friends not too.I truly believe this product should be recalled and thrown it the garbage.I am going to talk to a lawyer because i don't want to lose my vision.Clear eye, you stuck not a happy camper at all.I am normally a mild mannered woman, but you're messing with my beauty.Shame on you for continuing to sell the product and know something was wrong.God doesn't like evil and that's what you're doing if you continue to put this stuff on the market.Medication administered to or used by the patient: no.Patient counseling provided: unk.Relevant materials provided: none.Reporter name: (b)(6).
 
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Brand Name
CLEAR EYE
Type of Device
CLEAR EYE
MDR Report Key6204804
MDR Text Key63480672
Report NumberMW5066908
Device Sequence Number1
Product Code LPN
Number of Events Reported1
Summary Report (Y/N)N
Report Source Voluntary
Type of Report Initial
Report Date 11/07/2016
1 Device was Involved in the Event
1 Patient was Involved in the Event
Is this an Adverse Event Report? No
Is this a Product Problem Report? No
Device Operator No Information
Initial Date Manufacturer Received Not provided
Initial Date FDA Received12/23/2016
Type of Device Usage N
Patient Sequence Number1
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