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U.S. Department of Health and Human Services

MAUDE Adverse Event Report: EXCIMER LASER NONE

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EXCIMER LASER NONE Back to Search Results
Event Date 01/15/2005
Event Type  Injury  
Event Description

Fifteen years after undergoing corrective eye surgery at hospital, in the excimer laser program, i've developed severe dry eye, light sensitivity and a constant burning sensation in both eyes. Doctors have informed me these symptoms are likely a result of the procedure.

 
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Brand NameEXCIMER LASER
Type of DeviceNONE
MDR Report Key1578385
Report NumberMW5014323
Device Sequence Number1
Product CodeLZS
Report Source Voluntary
Reporter Occupation Patient
Type of Report Initial
Report Date 01/11/2010
1 Device Was Involved in the Event
1 Patient Was Involved in the Event
Date FDA Received01/11/2010
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: 01/11/2010 Patient Sequence Number: 1
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