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U.S. Department of Health and Human Services

MAUDE Adverse Event Report: NOT A SPECIFIC PRODUCT LASIK

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NOT A SPECIFIC PRODUCT LASIK Back to Search Results
Event Date 05/01/2004
Event Type  Injury  
Event Description

Lasik surgery ruined my vision. Even though, i reported a severe case of dry eyes to both my eye doctor and the lasik surgeons, during the screening process, the doctors still told me, i was an ideal candidate for the surgery. Since the surgery, by 9:00 pm at night, i can barely keep my eyes open due to the dryness, regardless of how many eyedrops i put in my eyes all day long. Also, i now has double-vision in each eye. Yes, that's right, i see four of everything. Having this surgery done was the biggest mistake of my life and i got to pay for this! the doctors make you sign every waiver possible so that you can't sue them for ruining your eyesight.

 
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Brand NameNOT A SPECIFIC PRODUCT
Type of DeviceLASIK
MDR Report Key1335379
Report NumberMW5010181
Device Sequence Number1
Product CodeLZS
Report Source Voluntary
Reporter Occupation PATIENT
Type of Report Initial
Report Date 03/04/2009
1 Device Was Involved in the Event
1 Patient Was Involved in the Event
Date FDA Received03/04/2009
Is This An Adverse Event Report? Yes
Is This A Product Problem Report? No
Device Operator OTHER
Was Device Available For Evaluation? No
Is The Reporter A Health Professional? No

Patient TREATMENT DATA
Date Received: 03/04/2009 Patient Sequence Number: 1
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