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U.S. Department of Health and Human Services

MAUDE Adverse Event Report: LASER-ASSISTED IN SITU KERATOMILEUSIS - LASIK- EXAMINER LASER - WAVEFRONT

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LASER-ASSISTED IN SITU KERATOMILEUSIS - LASIK- EXAMINER LASER - WAVEFRONT Back to Search Results
Event Date 02/10/2005
Event Type  Injury  
Event Description

Post lasik dry eye - loss of tear production due to cornea nerve damage. This is a severe dry eye condition and serious and permanently debilitating illness. I suffer every day as a result of this condition. I feel i have been deceived by dr (b) (6) and dr (b) (6) of the (b) (6) eye care institute, (b) (6). They minimized the risks to lasik and are completely unable to fix the problem they created. Lasik permanently damaged my corneal nerves and i am unable to produce tears. This procedure should be removed from the market immediately.

 
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Brand NameLASER-ASSISTED IN SITU KERATOMILEUSIS - LASIK-
Type of DeviceEXAMINER LASER - WAVEFRONT
MDR Report Key1633068
Report NumberMW5015149
Device Sequence Number1
Product CodeLZS
Report Source Voluntary
Reporter Occupation Patient
Type of Report Initial
Report Date 03/11/2010
1 Device Was Involved in the Event
1 Patient Was Involved in the Event
Date FDA Received03/11/2010
Is This An Adverse Event Report? Yes
Is This A Product Problem Report? No
Device Operator Service Personnel

Patient TREATMENT DATA
Date Received: 03/11/2010 Patient Sequence Number: 1
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