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

MAUDE Adverse Event Report: LASIK NONE

  • 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 NONE Back to Search Results
Event Date 09/30/2005
Event Type  Injury  
Event Description

Rptr reports that he had laser surgery in 2005 and now he has double and blurring vision and has to use many eyedrops. Reporter states that dr will not see him, or honor the warranty that he has. In oct 2006 rptr states that he had to have plugs inserted for dry eyes and saw a specialist and was told he had a refraction and his eye was the shape of a football. In 2008, pt had "lasik surgery touch up". Rptr states that he had 7 f/u visits and was told that he had scar tissue and an astigmatism and would have to wear an eye patch on his right eye. Pt states that he now has to have glasses to see after paying thousands of dollars for lasik surgery.

 
Search Alerts/Recalls

  New Search  |  Submit an Adverse Event Report

Brand NameLASIK
Type of DeviceNONE
MDR Report Key1080832
Report NumberMW5007737
Device Sequence Number1
Product CodeLZS
Report Source Voluntary
Reporter Occupation Patient
Type of Report Initial
Report Date 07/24/2008
1 Device Was Involved in the Event
0 PatientS WERE Involved in the Event:
Date FDA Received07/24/2008
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

-
-