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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 04/22/2000
Event Type  Injury  
Event Description

The lasik procedure has left me with very little sight in the right eye and an on going and progressively worsening left eye problems. Scar tissue seems to have developed in the right eye over six years and as previously mentioned is doing the same in the left eye. I'm told by every ophthalmologist eye surgeon that there is no remedy.

 
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Brand NameLASIK
Type of DeviceNONE
MDR Report Key1944031
Report NumberMW5018731
Device Sequence Number1
Product CodeLZS
Report Source Voluntary
Reporter Occupation Patient
Type of Report Initial
Report Date 12/27/2010
1 Device Was Involved in the Event
1 Patient Was Involved in the Event
Date FDA Received12/27/2010
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: 12/27/2010 Patient Sequence Number: 1
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