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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 01/15/2009
Event Type  Injury  
Event Description

Had lasik eye surgery. Was not aware of the real impact of dry eye syndrome. After 6, doctor said i would recover to 'pre lasik condition'. It's been over a year. My eyes are very, very slightly better. I'm buying (b) (6) of drops and lube a year to keep my eyes moist. Every hour i'm putting in a drop because of the pain. Doctor has no response to correct this and does not take accountability. We need to make this more aware and find cause.

 
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Brand NameNA
Type of DeviceLASIK
MDR Report Key1633058
Report NumberMW5015143
Device Sequence Number1
Product CodeLZS
Report Source Voluntary
Reporter Occupation Patient
Type of Report Initial
Report Date 03/13/2010
1 Device Was Involved in the Event
1 Patient Was Involved in the Event
Date FDA Received03/13/2010
Is This An Adverse Event Report? Yes
Is This A Product Problem Report? No
Device Operator Service Personnel
Was Device Available For Evaluation? No
Is The Reporter A Health Professional? No

Patient TREATMENT DATA
Date Received: 03/13/2010 Patient Sequence Number: 1
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