• 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: K181026
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]
OsteoBridge Intramedullary Diaphysis Segment Fixation (IDSF) nails (femur) 2 11/06/2020 Merete Medical GmbH
OsteoBridge Intramedullary Diaphysis Segment Fixation (IDSF) nails (humerus) 2 11/06/2020 Merete Medical GmbH
OsteoBridge Intramedullary Diaphysis Segment Fixation (IDSF) nails (tibia) 2 11/06/2020 Merete Medical GmbH
-
-