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 
 3 
 4 
 5 
 6 
 7 
 8 
 9 
 10 
 > 
 
270 records meeting your search criteria returned- Product Code: KNW Product Problem: Device Contamination with Chemical or Other Material Report Date From: 01/1/2007
New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
BARD PERIPHERAL VASCULAR, INC. MARQUEE KIT 02/27/2024
BARD PERIPHERAL VASCULAR, INC. MARQUEE KIT 02/22/2024
BARD PERIPHERAL VASCULAR, INC. TREK BONE LESION BIOPSY KIT 02/16/2024
Unknown Manufacturer MISSION NEEDLE 02/16/2024
BARD PERIPHERAL VASCULAR, INC. TREK BONE LESION BIOPSY KIT 02/07/2024
BARD PERIPHERAL VASCULAR, INC. TREK BONE LESION BIOPSY KIT 02/07/2024
BARD PERIPHERAL VASCULAR, INC. TREK BONE LESION BIOPSY KIT 02/06/2024
BARD PERIPHERAL VASCULAR, INC. MARQUEE 02/06/2024
BARD PERIPHERAL VASCULAR, INC. MARQUEE 02/06/2024
BARD PERIPHERAL VASCULAR, INC. MARQUEE 02/06/2024
-
-