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U.S. Department of Health and Human Services

MAUDE Adverse Event Report: LASIK NONE

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LASIK NONE Back to Search Results
Device Problem Adverse Event Without Identified Device or Use Problem (2993)
Patient Problem Cataract (1766)
Event Date 09/08/2012
Event Type  Injury  
Event Description
I had lasik surgery approximately 12 years ago and now must undergo cataract surgery. I am all of (b)(6), which is relatively young for this type of surgery. My ophthalmologist attributes this to the lasik, though he cannot definitively confirm it. Lasik surgery approximately year 2000.
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Brand NameLASIK
Type of DeviceNONE
MDR Report Key2744622
MDR Text Key2973559
Report NumberMW5026853
Device Sequence Number1
Product Code LZS
Reporter Country CodeUS
Number of Events Reported1
Summary Report (Y/N)N
Report Source Voluntary
Reporter Occupation Patient
Type of Report Initial
Report Date 09/09/2012
1 Device was Involved in the Event
1 Patient was Involved in the Event
Date FDA Received09/09/2012
Is this an Adverse Event Report? Yes
Is this a Product Problem Report? No
Device Operator Other
Was Device Available for Evaluation? No
Is the Reporter a Health Professional? No

Patient Treatment Data
Date Received: 09/09/2012 Patient Sequence Number: 1