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U.S. Department of Health and Human Services

MAUDE Adverse Event Report: VISIX LASER

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VISIX LASER Back to Search Results
Event Date 08/22/2000
Event Type  Injury  
Event Description

I was damaged by lasik in my left eye in 2000. He finally admitted that i had a decentration and wrinkles in my flap, but that he didn't have the laser to fix the problem. I had to go to a specialist in another country, to try to get my eye fixed but it was damaged too bad and i had to receive a corneal transplant. Dr told me he would foot the bill or reimburse me for the surgeries that it would take to fix my eye, i believed him and never went to a lawyer. Once it came time to be reimbursed, he said he didn't remember saying that he would reimburse me, and my statute of limitations ran out. I never rec'd a dime from him. I had to foot the bill on this by myself. I lost my house from these high surgery bills and now have to live with a corneal transplant because of this dr. Not one time over the years has he ever dropped a call or a letter to see how my eye was doing. This guy shouldn't even be a dr in my opinion. He now has a clinic in another country, and i wonder how many other people he has damaged since me.

 
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Brand NameVISIX LASER
Type of DeviceLASER
MDR Report Key1057106
Report NumberMW5007223
Device Sequence Number1
Product CodeLZS
Report Source Voluntary
Reporter Occupation Other
Type of Report Initial
Report Date 06/05/2008
1 Device Was Involved in the Event
1 Patient Was Involved in the Event
Date FDA Received06/05/2008
Is This An Adverse Event Report? Yes
Is This A Product Problem Report? Yes
Device Operator Health Professional
Is The Reporter A Health Professional? No

Patient TREATMENT DATA
Date Received: 06/05/2008 Patient Sequence Number: 1
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