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

MAUDE Adverse Event Report: LASIK SURGERY LASIK 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
 

LASIK SURGERY LASIK SURGERY Back to Search Results
Lot Number LASIK
Event Date 12/21/2001
Event Type  Injury  
Event Description

I had lasik surgery in 2001. This was the worst decision i have ever made. My eyes became severely red, dry and irritated. I have seen over 9 eye doctors since 2001, have tried every available eye drop, over the counter and prescribed available. I take multiple vitamins to try and maintain the little eye health i have left. From inserting plugs constantly into my eyes, to having them removed because the water would drain down my face all day, i now have scar tissue on my right upper plug that makes this eye have a mucus film drain from it constantly. This procedure should be stopped now before anyone else has to deal with the constant struggles of everyday life after lasik surgery.

 
Search Alerts/Recalls

  New Search  |  Submit an Adverse Event Report

Brand NameLASIK SURGERY
Type of DeviceLASIK SURGERY
Manufacturer (Section D)
LASIK SURGERY
MDR Report Key2145741
Report NumberMW5021159
Device Sequence Number1
Product CodeLZS
Report Source Voluntary
Reporter Occupation Patient
Type of Report Initial
Report Date 06/26/2011
1 Device Was Involved in the Event
1 Patient Was Involved in the Event
Date FDA Received06/26/2011
Is This An Adverse Event Report? Yes
Is This A Product Problem Report? No
Device Operator Service Personnel
Device LOT NumberLASIK
Is The Reporter A Health Professional? No

Patient TREATMENT DATA
Date Received: 06/26/2011 Patient Sequence Number: 1
-
-