• 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 3 of 3 Results
510(K) Number: K103327
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]
System, Nuclear Magnetic Resonance Imaging - Product Usage: is a whole body magnetic resonance scann... 2 10/20/2020 FEI # 2126677
GE Healthcare, LLC
GE 1.5T Signa HDxt, 3.0T Signa HDxt, Signa Vibrant, HD23 Software and the following model numbers: 2... 2 09/23/2013 FEI # 2126677
GE Healthcare, LLC
GE Healthcare, Discovery MR750w 3.0T System. Part Number: 5352293. Product Usage: It is indica... 2 04/11/2013 FEI # 2126677
GE Healthcare, LLC
-
-