• 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 4 of 4 Results
510(K) Number: K183040
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]
Philips Zenition 70, System code 718133 - Product Usage: The devices are used for radiological guida... 2 05/08/2020 FEI # 1218950
Philips North America, LLC
Zenition 70, Model #718133 2 02/17/2022 FEI # 3002807880
PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.
Zenition 70. Product Code 718133. The devices are used for radiological guidance and visualization d... 2 04/21/2025 FEI # 3016618143
Philips North America Llc
Zenition 70. The device is to be used in health care facilities both inside and outside the operatin... 2 04/21/2025 FEI # 3000976525
Philips Medical Systems Nederland B.V.
-
-