• Decrease font size
  • Return font size to normal
  • Increase font size
U.S. Department of Health and Human Services

Manufacturer and User Facility Device Experience (MAUDE)

  • 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 
 3 
 4 
 5 
 6 
 7 
 8 
 9 
 10 
 > 
 
195 records meeting your search criteria returned- Product Code: KWY Product Problem: Corroded Report Date From: 01/1/2009

New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
ZIMMER BIOMET, INC. UNKNOWN M/L TAPER STEM 06/14/2019
DEPUY ORTHOPAEDICS INC US UNKNOWN HIP FEMORAL STEM 06/04/2019
SMITH & NEPHEW ORTHOPAEDICS LTD HEMI HEAD 46MM 05/23/2019
SMITH & NEPHEW ORTHOPAEDICS LTD HEMI HEAD 50MM 05/22/2019
DEPUY ORTHOPAEDICS INC US PINNACLE MTL INS NEUT40IDX60OD 05/21/2019
DEPUY ORTHOPAEDICS, INC. 1818910 UNKNOWN HIP FEMORAL STEM 05/07/2019
DEPUY ORTHOPAEDICS, INC. 1818910 UNKNOWN HIP FEMORAL STEM 05/03/2019
ZIMMER BIOMET, INC. M2A-T UNIV 2-HOLE SHL SZ 41/56 05/02/2019
DEPUY ORTHOPAEDICS, INC. 1818910 UNKNOWN HIP FEMORAL HEAD 04/23/2019
DEPUY ORTHOPAEDICS, INC. 1818910 UNKNOWN HIP FEMORAL STEM 04/05/2019
-
-