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U.S. Department of Health and Human Services

MAUDE Adverse Event Report: NONE LASIK

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NONE LASIK Back to Search Results
Event Date 12/14/2007
Event Type  Injury  
Event Description

I had lasik surgery - i am now dealing with significant dry eye which has compromised my ability to complete daily tasks, including the ability to work productively. The dry eye is, quite simply a disability for me. I really struggle in office environments with florescent lighting. While lasikplus - the company who did the surgery is still providing care to me, the consent process was, in my opinion, glossed over - involves the reading of a pamphlet only and a required signature-.

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Brand NameNONE
Type of DeviceLASIK
MDR Report Key1280733
Report NumberMW5009537
Device Sequence Number1
Product CodeLZS
Report Source Voluntary
Reporter Occupation PATIENT
Type of Report Initial
Report Date 01/05/2009
1 Device Was Involved in the Event
1 Patient Was Involved in the Event
Date FDA Received01/05/2009
Is This An Adverse Event Report? Yes
Is This A Product Problem Report? No
Device Operator OTHER
Is The Reporter A Health Professional? No

Date Received: 01/05/2009 Patient Sequence Number: 1