• 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 07/17/2003
Event Type  Injury  
Event Description

In 2003, i had lasik surgery. Since that time, i have experienced extreme dry eyes and eye pain. On many days i cannot see much at all. I have had medical treatment for the dry eyes and pain with minimal success; the eyes will feel somewhat better for a short time only to become near debilitating again. Dates of use: #1. 2003, #2. 2004. Diagnosis or reason for use: #1. To improve vision. #2. I don't actually remember why they "enhanced" by eyes.

Search Alerts/Recalls

  New Search  |  Submit an Adverse Event Report

Brand NameLASIK
Type of DeviceLASIK
MDR Report Key1125983
Report NumberMW5008019
Device Sequence Number1
Product CodeLZS
Report Source Voluntary
Reporter Occupation Patient
Type of Report Initial
Report Date 08/15/2008
1 Device Was Involved in the Event
1 Patient Was Involved in the Event
Date FDA Received08/15/2008
Is This An Adverse Event Report? Yes
Is This A Product Problem Report? No
Device Operator Health Professional
Was Device Available For Evaluation? No
Is The Reporter A Health Professional? No

Date Received: 08/15/2008 Patient Sequence Number: 1