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U.S. Department of Health and Human Services

MAUDE Adverse Event Report: ALCON LASER NONE

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ALCON LASER NONE Back to Search Results
Event Date 03/01/2007
Event Type  Other  
Event Description

Had lasik surgery in 2007. Immediately had dry eyes so bad that could not open them in the morning. Night time dry eyes still exists. Right eye was over corrected and now have lost ability to focus at all because of loss of accommodation. Morning vision is blurry in both eyes, but worse in right which takes several hours to begin to clear.

 
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Brand NameALCON LASER
Type of DeviceNONE
MDR Report Key1434840
Report NumberMW5012315
Device Sequence Number1
Product CodeLZS
Report Source Voluntary
Reporter Occupation PATIENT
Type of Report Initial
Report Date 08/05/2009
1 Device Was Involved in the Event
1 Patient Was Involved in the Event
Date FDA Received08/05/2009
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
Was the Report Sent to FDA? No
Is this a Reprocessed and Reused Single-Use Device? No

Patient TREATMENT DATA
Date Received: 08/05/2009 Patient Sequence Number: 1
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