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U.S. Department of Health and Human Services

MAUDE Adverse Event Report: NIDEK QUEST LASER SYSTEM

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NIDEK QUEST LASER SYSTEM Back to Search Results
Event Date 02/10/2006
Event Type  Other  
Event Description

Pe states after a second laser surgery, she experienced floaters in both eyes. Pe states that the doctor told her that the surgery did not cause the floaters. Reports that she went to her eye care doctor and was told that she had severe dry eyes, epithelial ingrowth, in her right eye and sahara sands in her left eye. States that the doctor who did the laser surgery did not find these problems and will not return her phone calls.

 
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Brand NameNIDEK QUEST
Type of DeviceLASER SYSTEM
MDR Report Key1307448
Report NumberMW5009887
Device Sequence Number1
Product CodeLZS
Report Source Voluntary
Reporter Occupation
Type of Report Initial
Report Date 02/09/2008
1 Device Was Involved in the Event
0 PatientS WERE Involved in the Event:
Date FDA Received02/09/2009
Is This An Adverse Event Report? No
Is This A Product Problem Report? No
Device Operator LAY USER/PATIENT
Is The Reporter A Health Professional? No

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