• 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 11/05/2007
Event Type  Injury  
Event Description

Lasik has permanently damaged my eyes. I suffer from chronic dry eye. My left eye cannot be corrected by glasses or contacts and the prescription varies dramatically throughout the day. I have punctal plugs, am on restasis, flaxseed oil, celluvisc, night masks, a humidifier, and i cannot wear eye makeup. Now i have a vitreous detachment.

 
Search Alerts/Recalls

  New Search  |  Submit an Adverse Event Report

Brand NameLASIK
Type of DeviceLASIK
MDR Report Key1374432
Report NumberMW5010949
Device Sequence Number1
Product CodeLZS
Report Source Voluntary
Reporter Occupation PATIENT
Type of Report Initial
Report Date 05/01/2009
1 Device Was Involved in the Event
1 Patient Was Involved in the Event
Date FDA Received05/01/2009
Is This An Adverse Event Report? Yes
Is This A Product Problem Report? No
Device Operator
Was Device Available For Evaluation? No
Is The Reporter A Health Professional? No

Patient TREATMENT DATA
Date Received: 05/01/2009 Patient Sequence Number: 1
-
-