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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
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
Report NumberMW5026853
Device Sequence Number1
Product CodeLZS
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
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