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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 12/01/2006
Event Type  Injury  
Event Description

Pt reports that after having laser/lasik surgery on both of her eyes, she can no longer see and this has caused her not to be able to obtain her driver's license.

 
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Brand NameLASIK
Type of DeviceNONE
MDR Report Key1052128
Report NumberMW5007009
Device Sequence Number1
Product CodeLZS
Report Source Voluntary
Reporter Occupation Patient
Type of Report Initial
Report Date 05/27/2008
1 Device Was Involved in the Event
0 PatientS WERE Involved in the Event:
Date FDA Received05/27/2008
Is This An Adverse Event Report? Yes
Is This A Product Problem Report? No
Device Operator Service Personnel
Is The Reporter A Health Professional? No

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