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

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 
 > 
 
157 records meeting your search criteria returned- Product Code: LPH Product Problem: Unintended Movement Report Date From: 01/1/2009

New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
BIOMET UK LTD. UNKNOWN CEMENTLESS UKR 12/07/2020
STRYKER ORTHOPAEDICS-MAHWAH UNKNOWN ACCOLADE II FEMORAL STEM 10/19/2020
SMITH & NEPHEW, INC. COCR 12/14 FEM HEAD 26 + 0 10/08/2020
ZIMMER MANUFACTURING B.V. LINER STANDARD 3.5 MM OFFSET 36 MM I.D. 10/08/2020
STRYKER ORTHOPAEDICS-MAHWAH SIZE 5 ACCOLADE II 127 DEG 10/07/2020
ZIMMER MANUFACTURING B.V. SHELL POROUS WITH CLUSTER HOLES 56 MM O. 09/03/2020
BIOMET UK LTD. CER BIOLOXD OPTION HD 28MM 09/01/2020
DEPUY ORTHOPAEDICS INC US PINNACLE SECTOR II CUP 50MM 08/14/2020
DEPUY ORTHOPAEDICS INC US S-ROM*SLEEVE PRX ZTT, 18B-LRG 08/13/2020
CONFORMIS, INC. ITOTAL HIP G2 08/11/2020
-
-