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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 04/01/2004
Event Type  Injury  
Event Description

Pt reports that after having lasik surgery, she had to go back to bifocal lenses due to decreased vision. In 2004-2006 pt states that she then went to monovision lenses. However, her vision continued to get worse and she now uses readers to read. Pt was refunded her money.

 
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Brand NameLASIK
Type of DeviceNONE
MDR Report Key1179163
Report NumberMW5008430
Device Sequence Number1
Product CodeLZS
Report Source Voluntary
Reporter Occupation Patient
Type of Report Initial
Report Date 09/30/2008
1 Device Was Involved in the Event
0 PatientS WERE Involved in the Event:
Date FDA Received09/30/2008
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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