• 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 
 > 
 
356 records meeting your search criteria returned- Product Code: LPH Product Problem: Device Contaminated During Manufacture or Shipping Report Date From: 01/1/2009

New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
ZIMMER BIOMET, INC. ACT ARTIC HD ARCOM XL 28X42MM 11/24/2021
ZIMMER BIOMET, INC. TPRLC XR T1 PPS 13X146MM MM T1 11/07/2021
DEPUY ORTHOPAEDICS INC US SUMMIT POR TAPER SZ10 STD OFF 10/27/2021
DEPUY ORTHOPAEDICS INC US SUMMIT POR TAPER SZ10 HI OFF 10/27/2021
ZIMMER BIOMET, INC. TPRLC XR FP TYPE1 PPS 7X134MM 10/21/2021
ZIMMER BIOMET, INC. LINER NEUTRAL 36 MM I.D. SIZE II FOR USE 10/14/2021
ZIMMER BIOMET, INC. TPRLC XR MP T1 PPS 15X115MM 10/01/2021
ZIMMER BIOMET, INC. TPRLC 133 FP TYPE1 PPS SO 4.0 09/07/2021
ZIMMER BIOMET, INC. TPRLC XR T1 PPS 14X148MM MM T1 09/07/2021
ZIMMER BIOMET, INC. TPRLC 133 T1 PPS HO 9X137MM 08/26/2021
-
-