• 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: K122234
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]
The OEC 9900 C-Arm is designed to provide fluoroscopic and spot-film images of the patient during di... 2 08/27/2020 Ge Healthcare
OEC 9900 Elite. MDL Numbers: D148942, D155043 2 01/20/2017 GE OEC Medical Systems, Inc
The OEC 9900 Elite mobile fluoroscopy system is designed to provide fluoroscopic and spot-film image... 2 01/09/2017 GE OEC Medical Systems, Inc
-
-