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 8 of 8 Results
510(K) Number: K151681
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]
IntelliVue MP50. Product Number: M8004A. 2 12/02/2025 FEI # 3016618143
Philips North America Llc
IntelliVue MP80. Product Number: M8008A. 2 12/02/2025 FEI # 3016618143
Philips North America Llc
IntelliVue MP40. Product Number: M8003A. 2 12/02/2025 FEI # 3016618143
Philips North America Llc
IntelliVue MP90. Product Number: M8010A. 2 12/02/2025 FEI # 3016618143
Philips North America Llc
IntelliVue MP60. Product Number: M8005A. 2 12/02/2025 FEI # 3016618143
Philips North America Llc
IntelliVue MP70. Product Number: M8007A. 2 12/02/2025 FEI # 3016618143
Philips North America Llc
IntelliVue G7m Anesthesia Gas Module, Product Number 866173 2 10/01/2024 FEI # 3006648320
Philips North America
IntelliVue G7m Anesthesia Gas Module, Model no. 866173, Firmware Version 04.12.00, System Codes 4535... 2 07/23/2020 FEI # 1218950
Philips North America, LLC
-
-