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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
Device Problem Insufficient Information (3190)
Patient Problems Visual Disturbances (2140); Halo (2227)
Event Date 07/01/2004
Event Type  Injury  
Event Description

Lasik surgery followed by continuing glare and halo problems since the surgery.

 
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Type of DeviceLASIK SURGERY
MDR Report Key2280291
MDR Text Key2281697
Report NumberMW5022478
Device Sequence Number1
Product Code LZS
Combination Product (Y/N)
Reporter Country CodeUS
Number of Events Reported1
Summary Report (Y/N)N
Report Source Voluntary
Reporter Occupation PATIENT
Type of Report Initial
Report Date 09/30/2011
1 Device Was Involved in the Event
1 Patient Was Involved in the Event
Date FDA Received09/30/2011
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? Yes
Was the Report Sent to FDA? No

Patient TREATMENT DATA
Date Received: 09/30/2011 Patient Sequence Number: 1
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