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U.S. Department of Health and Human Services

MAUDE Adverse Event Report: LASIK SURGERY NONE

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LASIK SURGERY NONE Back to Search Results
Event Date 09/01/2008
Event Type  Injury  
Event Description

Five years post lasik surgery began progressive and severe night vision, i do not drive at night except in a well lit city. Had bilateral lasik 2002, at the time no problems. I receive annual eye exams. Last exam (b)(6) 2010. (b)(6).

 
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Brand NameLASIK SURGERY
Type of DeviceNONE
MDR Report Key1950873
Report NumberMW5018832
Device Sequence Number1
Product CodeLZS
Report Source Voluntary
Reporter Occupation Patient
Type of Report Initial
Report Date 12/31/2010
1 Device Was Involved in the Event
1 Patient Was Involved in the Event
Date FDA Received12/31/2010
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? Yes

Patient TREATMENT DATA
Date Received: 12/31/2010 Patient Sequence Number: 1
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