• 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 2 of 2 Results
510(K) Number: K083517
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 IntelliVue MP2 Patient Monitors (865040) - Product Usage: intended for monitoring and record... 2 12/08/2020 Philips North America Llc
Philips M8102A IntelliVue MP2 Model: 865040 Indicated for use by health care professionals wheneve... 2 09/29/2010 Philips Healthcare Inc.
-
-