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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 01/11/2007
Event Type  Injury  
Event Description

Received lasik laser surgery on my eye. Since that time, my eyesight has deteriorated terribly and i have permanent blurred and foggy vision. Diagnosis or reason for use: to improve eyesight. Event abated after use stopped or dose reduced: no.

 
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Type of DeviceLASIK
MDR Report Key1111792
Report NumberMW5007975
Device Sequence Number1
Product CodeLZS
Report Source Voluntary
Reporter Occupation RISK MANAGER
Type of Report Initial
Report Date 08/12/2008
1 Device Was Involved in the Event
1 Patient Was Involved in the Event
Date FDA Received08/12/2008
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? Yes

Patient TREATMENT DATA
Date Received: 08/12/2008 Patient Sequence Number: 1
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