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U.S. Department of Health and Human Services

MAUDE Adverse Event Report: LASIK

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LASIK Back to Search Results
Device Problem Insufficient Information (3190)
Patient Problems Dry Eye(s) (1814); Visual Impairment (2138)
Event Type  Injury  
Event Description

Severe dry eyes night vision problems.

 
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Brand NameLASIK
Type of DeviceLASIK
MDR Report Key2045913
MDR Text Key1885497
Report NumberMW5020170
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
Type of Report Initial
Report Date 04/03/2011
1 Device Was Involved in the Event
1 Patient Was Involved in the Event
Date FDA Received04/03/2011
Is This An Adverse Event Report? No
Is This A Product Problem Report? No
Device Operator HEALTH PROFESSIONAL
Was Device Available For Evaluation? No
Is The Reporter A Health Professional? No

Patient TREATMENT DATA
Date Received: 04/03/2011 Patient Sequence Number: 1
Treatment
LASIK
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