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 
 
 
11 records meeting your search criteria returned- Product Code: LGZ Product Problem: Failure of Device to Self-Test Report Date From: 01/1/2009
New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
OAKDALE LEVEL 1 HOTLINE FLUID WARMER, 390 09/20/2023
ST PAUL LEVEL 1 HOTLINE BLOOD AND FLUID WARMER 08/26/2022
OAKDALE LEVEL 1 HOTLINE FLUID WARMER, 390 06/14/2022
OAKDALE LEVEL 1 HOTLINE FLUID WARMER 05/25/2022
ST PAUL LEVEL ONE 07/15/2021
SMITHS MEDICAL ASD, INC. LEVEL 1 FAST-FLOW FLUID WARMER ACCESSORI 06/12/2020
ST PAUL LEVEL 1 HOTLINE FLUID WARMER 04/29/2020
ST PAUL LEVEL 1 HOTLINE FLUID WARMER 04/29/2020
SMITHS MEDICAL ASD; INC. LEVEL 1® HOTLINE® BLOOD AND FLUID WARMER 06/14/2019
SMITHS MEDICAL ASD; INC. LEVEL 1® HOTLINE® BLOOD AND FLUID WARMER 06/14/2019
-
-