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U.S. Department of Health and Human Services

MAUDE Adverse Event Report: BAUSCH & LOMB VISX LASIK

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BAUSCH & LOMB VISX LASIK Back to Search Results
Model Number VISIX
Event Date 09/09/2005
Event Type  Injury  
Event Description

Permanent blurred vision and dry eye, due to lasik surgery.

 
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Brand NameVISX
Type of DeviceLASIK
Manufacturer (Section D)
BAUSCH & LOMB
MDR Report Key1513537
Report NumberMW5013093
Device Sequence Number1
Product CodeLZS
Report Source Voluntary
Reporter Occupation PATIENT
Type of Report Initial
Report Date 10/06/2009
1 Device Was Involved in the Event
1 Patient Was Involved in the Event
Date FDA Received10/16/2009
Is This An Adverse Event Report? Yes
Is This A Product Problem Report? Yes
Device Operator HEALTH PROFESSIONAL
Device MODEL NumberVISIX
Was Device Available For Evaluation? Yes
Is The Reporter A Health Professional? No
Is this a Reprocessed and Reused Single-Use Device? No

Patient TREATMENT DATA
Date Received: 10/16/2009 Patient Sequence Number: 1
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