• Decrease font size
  • Return font size to normal
  • Increase font size
U.S. Department of Health and Human Services

MAUDE Adverse Event Report: LASIK SURGERY

  • Print
  • Share
  • E-mail
Super Search Devices@FDA
510(k) | DeNovo | Registration & Listing | Adverse Events | Recalls | PMA | HDE | Classification | Standards
CFR Title 21 | Radiation-Emitting Products | X-Ray Assembler | Medsun Reports | CLIA | TPLC

LASIK SURGERY Back to Search Results
Event Date 09/15/2005
Event Type  Injury  
Event Description

I had lasik eye surgery in 2003, enhancement surgery in the right eye in 2005. I had epithelial cell ingrowth in the right eye after the enhancement surgery. I had a third surgery in the right eye in 2006. I have been left with blurred vision, ghosting, double vision, halos in the right eye.

Search Alerts/Recalls

  New Search  |  Submit an Adverse Event Report

MDR Report Key1513525
Report NumberMW5013087
Device Sequence Number1
Product CodeLZS
Report Source Voluntary
Reporter Occupation PATIENT
Type of Report Initial
Report Date 10/18/2009
1 Device Was Involved in the Event
1 Patient Was Involved in the Event
Date FDA Received10/18/2009
Is This An Adverse Event Report? Yes
Is This A Product Problem Report? No
Is The Reporter A Health Professional? No
Was the Report Sent to FDA? No
Is this a Reprocessed and Reused Single-Use Device? No

Date Received: 10/18/2009 Patient Sequence Number: 1