Quick Links: Skip to main page content Skip to Search Skip to Topics Menu Skip to Common Links
  • 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 9 of 9 Results
Related Medical Device Recalls
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]
Z-1486-2020 - Allura Exper FD Series. System codes 722003 722010 722022 722005 722011 722019 722001 722002 722006 722012 722008 722013 722020 722025 722015 722023 722038 889006 889016 889009 72... 2 03/13/2020 Philips North America, LLC
Z-1487-2020 - Integris Allura 15 & 12, monoplane (system code 722043) and biplane (system code 722044) 2 03/13/2020 Philips North America, LLC
Z-1488-2020 - Integris Allura 9, system codes 722018 722021 2 03/13/2020 Philips North America, LLC
Z-1489-2020 - MultiDiagnost Eleva, System codes 722030 722016 722017 708032 708036 708034 708037 708038 2 03/13/2020 Philips North America, LLC
Z-1494-2020 - Cardio Vascular-Allura Centron, system code 722400 2 03/13/2020 Philips North America, LLC
Z-1491-2020 - Poly G Integris H5000, System code 72246 2 03/13/2020 Philips North America, LLC
Z-1492-2020 - UroDiagnost Eleva, system code 708033 2 03/13/2020 Philips North America, LLC
Z-1493-2020 - Allura CV20, system code 722031 2 03/13/2020 Philips North America, LLC
Z-1490-2020 - OmniDiagnost Eleva System codes 708028 708027 2 03/13/2020 Philips North America, LLC
-
-