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 5 of 5 Results
510(K) Number: K160621
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]
SIGNA Pioneer, with affected software versions: PX25.0 to PX25.5, PX26.0, PX26.1, PX28.0 to PX28.4,... 2 08/02/2024 GE Medical Systems, LLC
SIGNA Pioneer Nuclear Magnetic Resonance Imaging System - Product Usage: is a whole body magnetic re... 2 01/28/2020 GE Healthcare, LLC
SIGNA Pioneer - Product Usage: is a whole body magnetic resonance scanner designed to support high r... 2 07/12/2021 GE Healthcare, LLC
SIGNA Pioneer nuclear magnetic resonance imaging system 2 10/16/2021 GE Healthcare, LLC
GE Healthcare MR superconducting magnets, a component of GE Healthcare SIGNA Pioneer System, nuclear... 2 02/09/2022 GE Healthcare, LLC
-
-