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

MAUDE Adverse Event Report: LASIK 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 LASIK Back to Search Results
Event Date 01/03/2011
Event Type  Injury  
Event Description

I had lasik 5 years back and it burns like "profanity". Feel i should commit suicide, got conjunctivitis and the conditions worsened. I'm fed up, using tears natural and a steroid. Please help.

 
Search Alerts/Recalls

  New Search  |  Submit an Adverse Event Report

Brand NameLASIK
Type of DeviceLASIK
Manufacturer (Section D)
LASIK
MDR Report Key5678257
Report NumberMW5062463
Device Sequence Number0
Product CodeLZS
Report Source Voluntary
Reporter Occupation Patient
Type of Report Initial
Report Date 05/22/2016
1 Device Was Involved in the Event
1 Patient Was Involved in the Event
Date FDA Received05/22/2016
Is This An Adverse Event Report? Yes
Device Operator NO INFORMATION
Was Device Available For Evaluation? No Answer Provided
Is The Reporter A Health Professional? No Answer Provided
Was the Report Sent to FDA?
Event Location No Information
Was Device Evaluated By Manufacturer? No Answer Provided
Is The Device Single Use? No Answer Provided
Is this a Reprocessed and Reused Single-Use Device?
Type of Device Usage

Patient TREATMENT DATA
Date Received: 05/22/2016 Patient Sequence Number: 1
-
-