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U.S. Department of Health and Human Services

MAUDE Adverse Event Report: LASIK

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LASIK Back to Search Results
Event Date 08/01/2004
Event Type  Injury  
Event Description

Underwent lasik surgery and now have impaired vision as a result of starburst and halos.

 
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Type of DeviceLASIK
MDR Report Key1400305
Report NumberMW5011381
Device Sequence Number1
Product CodeLZS
Report Source Voluntary
Reporter Occupation PATIENT
Type of Report Initial
Report Date 06/07/2009
1 Device Was Involved in the Event
1 Patient Was Involved in the Event
Date FDA Received06/07/2009
Is This An Adverse Event Report? Yes
Is This A Product Problem Report? No
Device Operator OTHER
Was Device Available For Evaluation? No
Is The Reporter A Health Professional? Yes

Patient TREATMENT DATA
Date Received: 06/07/2009 Patient Sequence Number: 1
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