• 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 4 of 4 Results
PMA Number: P030047
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]
PRECISE PRO RX CAROTID STENT implant system, Product Codes: PC0520RXC, PC0530RXC, PC0540RXC, PC0620... 1 03/15/2021 Cordis Corporation
Cordis Precise Nitinol Stent System. The Cordis PRECISE Nitinol Stent System devices are designe... 2 12/20/2019 Cardinal Health Inc.
Cordis PRECISE (R) PRO RX Nitinol Stent System (Carotid) 2 06/10/2016 Cordis Corporation
Cordis PRECISE (R) RX Nitinol Stent System (Biliary) 2 06/10/2016 Cordis Corporation
-
-