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
 

 
 < 
 3 
 4 
 5 
 6 
 7 
 8 
 9 
 10 
 11 
 12 
 > 
 
180 records meeting your search criteria returned- Product Code: CBK Product Problem: Device Emits Odor Report Date From: 01/1/2007
New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
DRÄGERWERK AG & CO. KGAA EVITA XL 03/01/2017
COVIDIEN 840 VENTILATOR 02/24/2017
COVIDIEN 840 VENTILATOR 02/23/2017
HAMILTON MEDICAL, INC. HAMILTON-G5 02/22/2017
COVIDIEN 840 VENTILATOR 02/01/2017
COVIDIEN 840 VENTILATOR 01/30/2017
COVIDIEN 840 VENTILATOR 01/27/2017
RESPIRONICS CALIFORNIA, INC V200 VENTILATOR 01/16/2017
DRÄGERWERK AG & CO. KGAA FABIUS GS 01/13/2017
DRÄGERWERK AG & CO. KGAA EVITA XL 01/12/2017
-
-