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U.S. Department of Health and Human Services

MAUDE Adverse Event Report: LASIK SURGERY

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LASIK SURGERY Back to Search Results
Event Date 09/01/2002
Event Type  Injury  
Event Description

I had lasik surgery in 2001; a year later, my vision had worsened, so i had to have it again; to this date; i cannot see anything without rigid gas permeable contact lens that i can only wear for 8 hours a day; i'm literally blind without these glasses; i only wish i'd never gotten this surgery, because glasses don't even work. I'm really sad and depressed about this.

 
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Brand NameLASIK SURGERY
Type of DeviceLASIK
MDR Report Key1078776
Report NumberMW5007719
Device Sequence Number1
Product CodeLZS
Report Source Voluntary
Reporter Occupation Physician
Type of Report Initial
Report Date 07/20/2008
1 Device Was Involved in the Event
1 Patient Was Involved in the Event
Date FDA Received07/20/2008
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? Yes
Is this a Reprocessed and Reused Single-Use Device? No

Patient TREATMENT DATA
Date Received: 07/20/2008 Patient Sequence Number: 1
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