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

Medical Device Recalls

  • Print
  • Share
  • E-mail
-
1 to 3 of 3 Results
510(K) Number: K141079
Results per Page
New Searchexport reports to excelExport to Excel | HelpHelp
Product Description
Sort by Product Name [A-Z]
Sort by Product Name [Z-A]
Recall
Class
Sort by Recall Class [0-9]
Sort by Recall Class [9-0]
FDA Recall
Posting Date
Sort by Date Classified [0-9]
Sort by Date Classified [9-0]
Recalling Firm
Sort by Recalling Firm [A-Z]
Sort by Recalling Firm [Z-A]
OptiMedica Catalys Precision Laser System, CE 0044 containing software cOS 5.00.33 Product Label ... 2 10/03/2018 Johnson & Johnson Surgical Vision Inc
Catalys Precision Laser System-Catalys - U - US product; Catalys-1 - International product; software... 2 05/28/2015 Optimedica Corporation
OptiMedica Catalys Precision Laser System; Model No(s). Catalys-U (US), and Catalys-I (Outside US). ... 2 04/23/2015 Abbott Medical Optics, Inc.
-
-