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U.S. Department of Health and Human Services

MAUDE Adverse Event Report: UNKNOWN LASIK UNKNOWN

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UNKNOWN LASIK UNKNOWN Back to Search Results
Lot Number UNKNOWN
Event Date 08/11/2009
Event Type  Injury  
Event Description

I had lasik eye surgery in (b)(6) 2009. Two weeks later i started to suffer with severe headaches and severe eye pain, in addition i had sudden vision regression. I have been seeing a neuro-ophthalmologist at the (b)(6) for my condition. I have been diagnosed with a rare form of corneal neuropathy pain from lasik.

 
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Brand NameLASIK
Type of DeviceUNKNOWN
Manufacturer (Section D)
UNKNOWN
unknown
unknown
MDR Report Key2359430
Report NumberMW5023293
Device Sequence Number1
Product CodeLZS
Report Source Voluntary
Reporter Occupation Patient
Type of Report Initial
Report Date 11/30/2011
1 Device Was Involved in the Event
1 Patient Was Involved in the Event
Date FDA Received11/30/2011
Is This An Adverse Event Report? Yes
Is This A Product Problem Report? No
Device Operator Service Personnel
Device LOT NumberUNKNOWN
Was Device Available For Evaluation? No
Is The Reporter A Health Professional? No

Patient TREATMENT DATA
Date Received: 11/30/2011 Patient Sequence Number: 1
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