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U.S. Department of Health and Human Services

MAUDE Adverse Event Report: INTRALASE/WAVEFRONT LASIK NONE

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INTRALASE/WAVEFRONT LASIK NONE Back to Search Results
Event Date 07/30/2009
Event Type  Injury  
Event Description

Complications from intralase/wavefront lasik. Constant eyestrain, light sensitivity, loss of contrast sensitivity, eye pain, decreased quality of vision despite being "20/20". Upset about the type of advertising and lack of objectiveness of doctors in this area. Would love to see a mandatory unbiased second opinion for anyone considering lasik.

 
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Brand NameINTRALASE/WAVEFRONT LASIK
Type of DeviceNONE
MDR Report Key1522305
Report NumberMW5013321
Device Sequence Number1
Product CodeLZS
Report Source Voluntary
Reporter Occupation Patient
Type of Report Initial
Report Date 11/02/2009
1 Device Was Involved in the Event
0 PatientS WERE Involved in the Event:
Date FDA Received11/02/2009
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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