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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 09/09/2010
Event Type  Injury  
Event Description

Had lasik eye surgery on (b)(6), 2010. Now cannot see to do any of my daily tasks. Near and mid-vision are gone. I only see far away. Was only told i would need readers for the computer. Local doctor can't believe how farsighted they made me. I am preparing to commit suicide after i get me affairs in order for my children. Only those who have gone through this nightmare understand the guilt and shame. You spend thousands of dollars and have no recourse whatsoever when the outcome is bad. It is a great scam for the lasik centers. Where on earth could you buy a product and then not have any recourse if it does not work??? please put a stop to this before others die or ruin their lives!!! please listen to us!!!.

 
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Brand NameLASIK
Type of DeviceNONE
MDR Report Key1905783
Report NumberMW5018250
Device Sequence Number1
Product CodeLZS
Report Source Voluntary
Reporter Occupation Patient
Type of Report Initial
Report Date 11/16/2010
1 Device Was Involved in the Event
0 PatientS WERE Involved in the Event:
Date FDA Received11/16/2010
Is This An Adverse Event Report? Yes
Is This A Product Problem Report? No
Device Operator Service Personnel
Was Device Available For Evaluation? No

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