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 5 of 5 Results
510(K) Number: K120206
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]
Paradigm Insulin Pump (MMT-712, MMT-715) 2 04/02/2026 FEI # 3003166194
Medtronic MiniMed, Inc.
Paradigm REF: MMT-712 and MMT-715 2 03/03/2025 FEI # 3003166194
Medtronic MiniMed, Inc.
MiniMed Paradigm Insulin pump, model number MMT-712 2 03/26/2020 FEI # 3003166194
Medtronic MiniMed
MiniMed Paradigm 512 Insulin pump 2 03/26/2020 FEI # 3003166194
Medtronic MiniMed
Medtronic MiniMed Paradigm Insulin pump, model numbers MMT 515 and MMT-715 2 03/26/2020 FEI # 3003166194
Medtronic MiniMed
-
-