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 4 of 4 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-1317-2026 - Spectral CT; Product Code (REF): 728333; 2 02/06/2026 FEI # 3016618143
Philips North America Llc
Z-1318-2026 - Spectral CT 7500 on Rails; Product Code (REF): 728334; 2 02/06/2026 FEI # 3016618143
Philips North America Llc
Z-1316-2026 - IQon Spectral CT; Product Code (REF): 728332; 2 02/06/2026 FEI # 3016618143
Philips North America Llc
Z-1315-2026 - Brilliance iCT; Product Code (REF): 728306; 2 02/06/2026 FEI # 3016618143
Philips North America Llc
-
-