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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 06/11/2007
Event Type  Injury  
Event Description

Halos during night & day, dryness / irritation of eyes always.

 
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Type of DeviceLASIK
MDR Report Key1282209
Report NumberMW5009557
Device Sequence Number1
Product CodeLZS
Report Source Voluntary
Reporter Occupation PATIENT
Type of Report Initial
Report Date 01/07/2009
1 Device Was Involved in the Event
1 Patient Was Involved in the Event
Date FDA Received01/07/2009
Is This An Adverse Event Report? Yes
Is This A Product Problem Report? Yes
Device Operator HEALTH PROFESSIONAL
Was Device Available For Evaluation? Device Returned To Manufacturer
Date Returned to Manufacturer02/07/2008
Is The Reporter A Health Professional? No

Patient TREATMENT DATA
Date Received: 01/07/2009 Patient Sequence Number: 1
Treatment
LASIK
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