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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 09/01/2006
Event Type  Injury  
Event Description

Pt states that after having lasix surgery, she started to have "black spots and smoke trails" in her vision. Her doctor told her that her vision was over corrected.

 
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Brand NameLASIK
Type of DeviceNONE
MDR Report Key1047149
Report NumberMW5006915
Device Sequence Number1
Product CodeLZS
Report Source Voluntary
Reporter Occupation Patient
Type of Report Initial
Report Date 05/16/2008
1 Device Was Involved in the Event
0 PatientS WERE Involved in the Event:
Date FDA Received05/16/2008
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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