• 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 5 of 5 Results
510(K) Number: K945945
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]
T5-NT, Model 78104 Product Usage: Indicated for use as a diagnostic device. It can produce cross... 2 04/18/2018 Philips Electronics North America Corporation
ACS-NT, Model 78108 Product Usage: Indicated for use as a diagnostic device. It can produce cros... 2 04/18/2018 Philips Electronics North America Corporation
T10-NT, Model 78107 Product Usage: Indicated for use as a diagnostic device. It can produce cros... 2 04/18/2018 Philips Electronics North America Corporation
SENSE Body Coil 1.5T with identification; used in the ACS NT, Intera 1.5T and Achieva 1.5T MR syste... 2 02/26/2016 Philips Electronics North America Corporation
Gyroscan MRI 2 06/27/2007 Philips Medical Systems North America Co. Phillips
-
-