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U.S. Department of Health and Human Services

MAUDE Adverse Event Report: N/A LASIK

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N/A LASIK Back to Search Results
Device Problem Insufficient Information (3190)
Patient Problems Corneal Edema (1791); Visual Impairment (2138)
Event Type  Injury  
Event Description

I had lasik and now have ectasia. My vision changes every six months.

 
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Brand NameN/A
Type of DeviceLASIK
MDR Report Key2163552
MDR Text Key2098366
Report NumberMW5021316
Device Sequence Number1
Product Code LZS
Combination Product (Y/N)
Reporter Country CodeUS
Number of Events Reported1
Summary Report (Y/N)N
Report Source Voluntary
Reporter Occupation PATIENT
Type of Report Initial
Report Date 07/11/2011
1 Device Was Involved in the Event
1 Patient Was Involved in the Event
Date FDA Received07/11/2011
Is This An Adverse Event Report? Yes
Is This A Product Problem Report? No
Device Operator OTHER
Was Device Available For Evaluation? Yes
Is The Reporter A Health Professional? Yes

Patient TREATMENT DATA
Date Received: 07/11/2011 Patient Sequence Number: 1
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