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U.S. Department of Health and Human Services

MAUDE Adverse Event Report: LASIK EYE SURGERY NONE

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LASIK EYE SURGERY NONE Back to Search Results
Event Date 01/16/2006
Event Type  Injury  
Event Description

I had laser eye surgery to correct nearsightedness and astigmatism. The dr attempted to give me some vision for the mid-range distance in my right eye because i teach children computer technology and i needed to see their screens. He said he did this by not exactly correcting the eye to 20/20. The left eye was supposedly corrected to be normal 20/20. As it turned out, the right eye is pretty good at 20/30. The left eye is bad. It was bad to the point that i had it done by the same doctor one year after the first surgery. It is now worse than the first time. I have worse triple vision, fuzziness and bad halo effect. I also have very dry eyes especially in the morning when i wake up and can barely open my eyes.

 
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Brand NameLASIK EYE SURGERY
Type of DeviceNONE
MDR Report Key1310516
Report NumberMW5009913
Device Sequence Number1
Product CodeLZS
Report Source Voluntary
Reporter Occupation PATIENT
Type of Report Initial
Report Date 02/09/2009
1 Device Was Involved in the Event
0 PatientS WERE Involved in the Event:
Date FDA Received02/09/2009
Is This An Adverse Event Report? Yes
Is This A Product Problem Report? No
Device Operator OTHER
Is The Reporter A Health Professional? No

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