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U.S. Department of Health and Human Services

MAUDE Adverse Event Report: LASIK

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LASIK Back to Search Results
Event Date 12/05/2005
Event Type  Injury  
Event Description

Permanent visual problems resulting from lasik procedure. I was 20/20 with contacts prior to the procedure, and had no eye problems. I now suffer from higher order aberrations as well as dry eye. I have lost my best corrected vision and can no longer wear contact lenses, due to discomfort. This procedure has severely impacted my quality of life.

 
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Type of DeviceLASIK
MDR Report Key1128165
Report NumberMW5008037
Device Sequence Number1
Product CodeLZS
Report Source Voluntary
Reporter Occupation Patient
Type of Report Initial
Report Date 08/19/2008
1 Device Was Involved in the Event
1 Patient Was Involved in the Event
Date FDA Received08/19/2008
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

Patient TREATMENT DATA
Date Received: 08/19/2008 Patient Sequence Number: 1
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