• 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 
 3 
 4 
 5 
 6 
 7 
 8 
 9 
 10 
 > 
 
112 records meeting your search criteria returned- Product Code: KWA Product Problem: Tear, Rip or Hole in Device Packaging Report Date From: 01/1/2015
New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
ZIMMER BIOMET, INC. TLOC 133 MP SP T1 PPSHO 6X97.5 12/14/2020
ZIMMER BIOMET, INC. TPRLC 133 T1 PPS SO 17X154MM T1 11/17/2020
ZIMMER BIOMET, INC. TPRLC 133 T1 PPS SO 18X156MM T1 11/17/2020
ZIMMER BIOMET, INC. ARCOS BRCH SZ A HI 60MM 11/03/2020
ZIMMER BIOMET, INC. ARCOS BRCH SZ B HI 60MM 11/03/2020
ZIMMER BIOMET, INC. ARCOS BRCH SZ C HI 60MM 11/03/2020
ZIMMER BIOMET, INC. ARCOS CON SZ D HI 80MM 11/03/2020
ZIMMER BIOMET, INC. ARCOS CON SZ E STD 80MM 11/03/2020
ZIMMER BIOMET, INC. ARCOS CAL SZ A +0 HI 50MM 11/03/2020
ZIMMER BIOMET, INC. ARCOS BRCH SZ E HI 60MM 11/03/2020
-
-