• 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: K981624
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]
Surgical Tools and Cardiovascular Specialty marketing brochures, Reference numbers: US-AS18-210002 ... 2 04/12/2024 Baxter Healthcare Corporation
Baxter Flo-Thru Intraluminal Shunt, Product Codes: a) Product Code FT12100, 1.00 GLOBAL; b) Prod... 2 01/05/2024 Baxter Healthcare Corporation
Flo-Thru Intraluminal Shunt. Used in coronary artery or peripheral vascular procedures. Used to shun... 2 04/29/2022 Baxter Healthcare Corporation
-
-