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 4 of 4 Results
510(K) Number: K960630
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]
Compact Speed Reducer, 60:1 2 05/04/2017 The Anspach Effort, Inc.
Compact Speed Reducer, 60:1 Black Max 2 05/04/2017 The Anspach Effort, Inc.
ANSPACH***REF 98-0044***Custom Device Speed Reducer with Bumper***Rx Only*** This device is inten... 2 06/25/2014 The Anspach Effort, Inc.
ANSPACH***REF 98-0048***Custom Circular ePLUS-FP***Rx Only*** This device is intended to be used ... 2 06/25/2014 The Anspach Effort, Inc.
-
-