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U.S. Department of Health and Human Services

MAUDE Adverse Event Report: LASIK NONE

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LASIK NONE Back to Search Results
Event Date 12/21/1996
Event Type  Injury  
Event Description

Dear sir/madam: please be informed that i had a lasik surgery in late 1996 at the hospital by a dr. I have written you a certified letter on 04/28/2008 in reference to the problem, and i have also written certified letters through the years to medical entities, and political officers. Dr did a malicious act by masking half of my cornea and created fluids under the cornea flap to conceal the immediate results. I have been all over the world to see if something can be done to correct my cornea, but nothing can be done. In my letter to you, i have enclosed tomographies, so you can see that only a human hand could have covered half of the cornea and create fluids under the flap. Currently, my cornea is irritated, i can't wear contact lenses, and i can see triple images. I hope your agency shall investigate this matter and bring dr. Mcdonald and other doctors like her to justice. If doctors like dr are left unchecked, the problems doctors injuring patients will not go away, and we will have an injured handicapped and unhealthy society. Sincerely.

Event Description

My right eye cornea and vitreous was intentionally injured. Prior to lasik surgery (that was anything but lasik surgery), i had myopic but healthy eye. Now, i am visually handicapped with half cornea treated, and a vitreous detachment. Dr has committed a malicious act and she shall be brought to justice. Doctors that commit these kinds of hideous malicious acts are capable of doing any criminal act.

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Brand NameLASIK
Type of DeviceNONE
MDR Report Key1038108
Report NumberMW5006696
Device Sequence Number1
Product CodeLZS
Report Source Voluntary
Reporter Occupation PATIENT
Type of Report Initial,Followup
Report Date 05/04/2008
1 Device Was Involved in the Event
1 Patient Was Involved in the Event
Date FDA Received05/04/2008
Is This An Adverse Event Report? Yes
Is This A Product Problem Report? No
Device Operator OTHER
Was Device Available For Evaluation? Yes
Is The Reporter A Health Professional? No
Is this a Reprocessed and Reused Single-Use Device? No

Date Received: 05/04/2008 Patient Sequence Number: 1