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U.S. Department of Health and Human Services

MAUDE Adverse Event Report: LASIK WITH WAVE

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LASIK WITH WAVE Back to Search Results
Event Date 06/20/2008
Event Type  Injury  
Event Description

Severe dry eyes from lasik with wave technology. For therapy, currently using nocturnally heavy lubricant eye ointment of 41. 5% mineral oil, 56. 8% white petrolatum with eye mask to preserve humidity. Daytime use of lubricating eye drops.

 
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Brand NameLASIK WITH WAVE
Type of DeviceLASIK WITH WAVE
MDR Report Key1134023
Report NumberMW5008079
Device Sequence Number1
Product CodeLZS
Report Source Voluntary
Reporter Occupation Patient
Type of Report Initial
Report Date 08/23/2008
1 Device Was Involved in the Event
1 Patient Was Involved in the Event
Date FDA Received08/23/2008
Is This An Adverse Event Report? Yes
Is This A Product Problem Report? No
Device Operator Health Professional
Was Device Available For Evaluation? No
Is The Reporter A Health Professional? No

Patient TREATMENT DATA
Date Received: 08/23/2008 Patient Sequence Number: 1
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