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 6 of 6 Results
Related Medical Device Recalls Recall Date to: 08/31/2015
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-0366-2007 - Philips Integris Allura x-ray systems angiographic - Allura 9 F/C (floor and ceiling models). A mono-plane analog Allura with a 9' Image Intensifier 2 01/25/2007 Philips Medical Systems North America Co. Phillips
Z-0371-2007 - FD 20/10 X-Ray System, Angiograph, biplane, digital Allura FD, 10' and 20' detectors 2 01/25/2007 Philips Medical Systems North America Co. Phillips
Z-0370-2007 - FD 10/10 X-Ray System, Angiograph, bi-plane digital Allura FD, 10' detector 2 01/25/2007 Philips Medical Systems North America Co. Phillips
Z-0367-2007 - Allura Mono X-Ray System, angiographic - monoplane, analog Allura with a 12' and 15' Image Intensifier 2 01/25/2007 Philips Medical Systems North America Co. Phillips
Z-0369-2007 - Allura FD20 x-ray system, angiograph, monoplane, digital Allura FD with a 20' detector FD 2 01/25/2007 Philips Medical Systems North America Co. Phillips
Z-0368-2007 - Allura FD 10 FC, X-Ray System, angiographic - a monoplane, digital Allura FD (flat detector) with a 10' Image Intensifier (II). 2 01/25/2007 Philips Medical Systems North America Co. Phillips
-
-