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U.S. Department of Health and Human Services

MAUDE Adverse Event Report: LASIK EYE SURGERY

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LASIK EYE SURGERY Back to Search Results
Event Date 01/01/2002
Event Type  Injury  
Event Description

I had lasik done in 2002 by (b)(6). I have had night time vision problems. Now i have eye pain from a problem flap. Reason for use: correction of nearsightedness.

 
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Brand NameLASIK EYE SURGERY
Type of DeviceLASIK EYE SURGERY
MDR Report Key2215666
Report NumberMW5021752
Device Sequence Number1
Product CodeLZS
Report Source Voluntary
Reporter Occupation Patient
Type of Report Initial
Report Date 08/11/2011
1 Device Was Involved in the Event
1 Patient Was Involved in the Event
Date FDA Received08/11/2011
Is This An Adverse Event Report? Yes
Is This A Product Problem Report? No
Device Operator Health Professional
Was Device Available For Evaluation? No
Is The Reporter A Health Professional? No
Is this a Reprocessed and Reused Single-Use Device? No

Patient TREATMENT DATA
Date Received: 08/11/2011 Patient Sequence Number: 1
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