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 10 of 114 Results
510(K) Number: K193215
 
 1 
 2 
 3 
 4 
 5 
 6 
 7 
 8 
 9 
 10 
 > 
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]
Intera Achieva 1.5T Pulsar; Product Number: 781171; 2 06/09/2025 Philips North America
Intera 1.5T Explorer/Nova Dual Product Number: 781108; 2 06/09/2025 Philips North America
Intera 1.5T Master/Nova Product Number: 781106; 2 06/09/2025 Philips North America
Intera 1.5T Omni/Stellar; Product Number: 781104; 2 06/09/2025 Philips North America
Intera 1.5T Achieva Nova Product Number: 781172; 2 06/09/2025 Philips North America
Intera 1.5T Achieva IT Nova Product Number: 781175 2 06/09/2025 Philips North America
Achieva XR Product Numbers: (1) 781153, (2) 781253; 2 06/09/2025 Philips North America
Intera 1.5T Achieva Nova-Dual Product Number: 781173; 2 06/09/2025 Philips North America
Product Name: Ingenia Elition X; Model Numbers: (1) 781358, (2) 782107, (3) 782136; 2 05/16/2025 Philips North America Llc
Product Name: Ingenia Elition S; Model Numbers: (1) 781357, (2) 782106, (3) 782137; 2 05/16/2025 Philips North America Llc
-
-