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U.S. Department of Health and Human Services

MAUDE Adverse Event Report: LASIK NONE

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LASIK NONE Back to Search Results
Event Date 05/01/2004
Event Type  Injury  
Event Description

In 2004, i had lasik eye. The surgery never completely worked and left me with dry eyes, cornea scaring, cataracts, and a detached retina, which was due to the thinning of my retina during lasik. I also had a temporary cornea edema. Per my current ophthalmologist, these were all side effects of the surgery, something my original doctor never told me could result from the surgery. These factors have left me with limited and impaired vision.

 
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Brand NameLASIK
Type of DeviceNONE
MDR Report Key1513530
Report NumberMW5013092
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? No
Is The Reporter A Health Professional? No

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