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

MAUDE Adverse Event Report: LASER EYE 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
 

LASER EYE SURGERY Back to Search Results
Event Date 04/20/2007
Event Type  Injury  
Event Description

I had lasik surgery. I have been having dry eye with pain in the right eye. Sometimes the pain is really bad and other it is tolerate. I just want no one to go through this kind of daily pain. Drs should have to give more info on the side effects of this procedure.

 
Search Alerts/Recalls

  New Search  |  Submit an Adverse Event Report

Brand NameUnknown Brand Name
Type of DeviceLASER EYE SURGERY
MDR Report Key2344264
Report NumberMW5023145
Device Sequence Number1
Product CodeLZS
Report Source Voluntary
Reporter Occupation Patient
Type of Report Initial
Report Date 11/15/2011
1 Device Was Involved in the Event
1 Patient Was Involved in the Event
Date FDA Received11/15/2011
Is This An Adverse Event Report? Yes
Is This A Product Problem Report? No
Device Operator Service Personnel
Is The Reporter A Health Professional? No

Patient TREATMENT DATA
Date Received: 11/15/2011 Patient Sequence Number: 1
-
-