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U.S. Department of Health and Human Services

MAUDE Adverse Event Report: WAVEFRONT LASIK SURGERY

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WAVEFRONT LASIK SURGERY Back to Search Results
Event Date 04/29/2008
Event Type  Injury  
Event Description

I had lasik done in one eye. For days post lasik i started to have recurrent cornea erosions and dry eye. I never had any problems with my eye before. The agony and pain i have experienced has meant that i have not been able to work and my life right now resolves around trying to lessen the pain.

 
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Brand NameWAVEFRONT LASIK SURGERY
Type of DeviceLASIK SURGERY
MDR Report Key1058388
Report NumberMW5007241
Device Sequence Number1
Product CodeLZS
Report Source Voluntary
Reporter Occupation Other
Type of Report Initial
Report Date 06/06/2008
1 Device Was Involved in the Event
0 PatientS WERE Involved in the Event:
Date FDA Received06/06/2008
Is This An Adverse Event Report? Yes
Is This A Product Problem Report? No
Device Operator Service Personnel
Is The Reporter A Health Professional? No

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