• 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 01/11/2007
Event Type  Injury  
Event Description

Received lasik laser surgery on my eye. Since that time, my eyesight has deteriorated terribly and i have permanent blurred and foggy vision. Diagnosis or reason for use: to improve eyesight. Event abated after use stopped or dose reduced: no.

Search Alerts/Recalls

  New Search  |  Submit an Adverse Event Report

Type of DeviceLASIK
MDR Report Key1111792
Report NumberMW5007975
Device Sequence Number1
Product CodeLZS
Report Source Voluntary
Reporter Occupation RISK MANAGER
Type of Report Initial
Report Date 08/12/2008
1 Device Was Involved in the Event
1 Patient Was Involved in the Event
Date FDA Received08/12/2008
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? Yes

Date Received: 08/12/2008 Patient Sequence Number: 1