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

MAUDE Adverse Event Report: PRK 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
 

PRK SURGERY Back to Search Results
Event Date 11/30/2008
Event Type  Injury  
Event Description

I had prk surgery on my eye to correct vision. I now suffer from severe dry eye problems. I was not properly screened or warned before this elective surgery.

 
Search Alerts/Recalls

  New Search  |  Submit an Adverse Event Report

Type of DevicePRK SURGERY
MDR Report Key1293889
Report NumberMW5009654
Device Sequence Number1
Product CodeLZS
Report Source Voluntary
Reporter Occupation Patient
Type of Report Initial
Report Date 11/22/2009
1 Device Was Involved in the Event
1 Patient Was Involved in the Event
Date FDA Received01/22/2009
Is This An Adverse Event Report? Yes
Is This A Product Problem Report? No
Device Operator Service Personnel
Was Device Available For Evaluation? No
Is The Reporter A Health Professional? No

Patient TREATMENT DATA
Date Received: 01/22/2009 Patient Sequence Number: 1
-
-