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U.S. Department of Health and Human Services

MAUDE Adverse Event Report: LASER LASIK SURGERY NONE

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LASER LASIK SURGERY NONE Back to Search Results
Event Date 11/21/2008
Event Type  Injury  
Event Description

After lasik surgery, my vision at night has become a problem with halos so big it is affecting my night driving and depth perception. It only improved my actual vision from -6. 25 to -1. 25. After seven months since the surgery, the halos are the same and no improvement of my night vision. I am scared.

 
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Brand NameLASER LASIK SURGERY
Type of DeviceNONE
MDR Report Key1393845
Report NumberMW5011218
Device Sequence Number1
Product CodeLZS
Report Source Voluntary
Reporter Occupation PATIENT
Type of Report Initial
Report Date 05/25/2009
1 Device Was Involved in the Event
1 Patient Was Involved in the Event
Date FDA Received05/25/2009
Is This An Adverse Event Report? Yes
Is This A Product Problem Report? Yes
Device Operator OTHER
Was Device Available For Evaluation? No
Is The Reporter A Health Professional? No

Patient TREATMENT DATA
Date Received: 05/25/2009 Patient Sequence Number: 1
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