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U.S. Department of Health and Human Services

MAUDE Adverse Event Report: UNKNOX LASIK

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UNKNOX LASIK Back to Search Results
Event Date 10/22/1997
Event Type  Injury  
Event Description

I had lasik surgery. Immediately following the surgery, both eye flaps dislocated requiring a 2nd surgery to put back in place and suture them. For the past couple of years, my vision has been declining and i began seeking a solution in 2008. I was informed my corneas were severly "misshappen", i had extreme dry eyes, scar tissue on the corneas and cataracts on both eyes all resulting in very blurred vision.

 
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Brand NameLASIK
Type of DeviceLASIK
Manufacturer (Section D)
UNKNOX
MDR Report Key1513497
Report NumberMW5013061
Device Sequence Number1
Product CodeLZS
Report Source Voluntary
Reporter Occupation PATIENT
Type of Report Initial
Report Date 10/16/2009
1 Device Was Involved in the Event
1 Patient Was Involved in the Event
Date FDA Received10/16/2009
Is This An Adverse Event Report? Yes
Is This A Product Problem Report? No
Device Operator OTHER
Was Device Available For Evaluation? Yes
Is The Reporter A Health Professional? No

Patient TREATMENT DATA
Date Received: 10/16/2009 Patient Sequence Number: 1
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