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

MAUDE - Manufacturer and User Facility Device Experience
  • Print
  • Share
  • E-mail
-
Super Search Devices@FDA
510(k) | DeNovo | Registration & Listing | Adverse Events | Recalls | PMA | HDE | Classification | Standards
CFR Title 21 | Radiation-Emitting Products | X-Ray Assembler | Medsun Reports | CLIA | TPLC
 

 
 
 1 
 2 
 > 
 
16 records meeting your search criteria returned- Product Code: MEH Product Problem: Tear, Rip or Hole in Device Packaging Report Date From: 01/1/2009
New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
DEPUY IRELAND - 9616671 ACTIS COLLARED HIGH SIZE 7 05/18/2023
DEPUY IRELAND - 9616671 ACTIS COLLARED HIGH SIZE 7 12/28/2022
DEPUY IRELAND - 9616671 CORAIL AMT SZ8 135 LOW COL 12/15/2022
DEPUY IRELAND - 9616671 ACTIS COLLARED STD SIZE 9 06/27/2022
DEPUY IRELAND - 9616671 ACTIS COLLARED STD SIZE 6 04/25/2022
DEPUY IRELAND - 9616671 ACTIS COLLARED HIGH SIZE 5 04/18/2022
DEPUY IRELAND - 9616671 ACTIS COLLARED STD SIZE 6 12/29/2021
DEPUY IRELAND - 9616671 ACTIS COLLARED STD SIZE 4 08/24/2021
DEPUY IRELAND - 9616671 ACTIS COLLARED STD SIZE 5 05/21/2021
ZIMMER BIOMET, INC. FEMORAL STEM 12/14 NECK TAPER PLASMA SPR 05/06/2021
-
-