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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 09/15/2007
Event Type  Injury  
Event Description

Pt reports that she has had pain in both eyes since the lasik surgery. She is not able to work, her vision is decreased and sensitive to light.

 
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Brand NameLASIK
Type of DeviceNONE
MDR Report Key1047148
Report NumberMW5006914
Device Sequence Number1
Product CodeLZS
Report Source Voluntary
Reporter Occupation Other
Type of Report Initial
Report Date 05/19/2008
1 Device Was Involved in the Event
0 PatientS WERE Involved in the Event:
Date FDA Received05/19/2008
Is This An Adverse Event Report? Yes
Is This A Product Problem Report? No
Device Operator Lay User/Patient
Is The Reporter A Health Professional? No

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