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
 

 
 
7 records meeting your search criteria returned- Product Code: FCG Product Problem: Device Markings/Labelling Problem Report Date From: 01/1/2019

New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
BARD PERIPHERAL VASCULAR, INC. MAGNUM NEEDLE 11/14/2022
BARD PERIPHERAL VASCULAR, INC. MAGNUM NEEDLE 11/07/2022
CAREFUSION, INC JAMSHIDI (TJ) NEEDLE BONE MARROW 11G X4 10/03/2022
BARD PERIPHERAL VASCULAR, INC. MAGNUM NEEDLE 05/30/2022
BARD PERIPHERAL VASCULAR, INC. MAGNUM NEEDLE 04/05/2022
BARD PERIPHERAL VASCULAR, INC. MAGNUM NEEDLE 12/30/2021
BARD PERIPHERAL VASCULAR, INC. MAGNUM 12/23/2021
-
-