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

MAUDE Adverse Event Report: LASIK

  • 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 Back to Search Results
Event Date 11/07/2007
Event Type  Injury  
Event Description

I had lasik surgery and it pretty much ruined my quality of life. I now suffer from extremely painful dry eye syndrome. I never even knew what dry eye syndrome meant before my lasik surgery. I thought complications were a very, very small percent and now i am reading that the dry eye complications are huge. I think this surgery is a crime against those of us who think it is a miracle, only to find out that our lives are ruined with pain afterwards.

 
Search Alerts/Recalls

  New Search  |  Submit an Adverse Event Report

Type of DeviceLASIK
MDR Report Key1358375
Report NumberMW5010657
Device Sequence Number1
Product CodeLZS
Report Source Voluntary
Reporter Occupation Other
Type of Report Initial
Report Date 04/07/2009
1 Device Was Involved in the Event
1 Patient Was Involved in the Event
Date FDA Received04/07/2009
Is This An Adverse Event Report? Yes
Is This A Product Problem Report? No
Device Operator Service Personnel
Was Device Available For Evaluation? No
Is The Reporter A Health Professional? No

Patient TREATMENT DATA
Date Received: 04/07/2009 Patient Sequence Number: 1
-
-