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: K123392
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]
Avenir® Muller Stem Standard, uncemented HA, 1, Taper 12/14 Item Number: 01.06010.001 - Product Usag... 2 12/20/2018 FEI # 3005233524
Zimmer GmbH
Avenir M®ller Stem 4 Standard Avenir M®ller Stem 6 Lateral Hip joint metal/ceramic/polymer semi-... 2 07/26/2016 FEI # 3005233524
Zimmer Gmbh
Avenir Muller Stem; Item Number: 01.06010.104, Lot Number: 2905496, UDI: (01)00889024479500 (17)2204... 2 04/26/2018 FEI # 3005233524
Zimmer GmbH
Avenir Muller Stem; Item Number: 01.06010.003, Lot Number: 2904368, UDI: (01) 00889024479494 (17) 22... 2 04/26/2018 FEI # 3005233524
Zimmer GmbH
-
-