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
 

 
 < 
 2 
 3 
 4 
 5 
 6 
 7 
 8 
 9 
 10 
 11 
 > 
 
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
RESPIRONICS CALIFORNIA, INC ESPRIT VENTILATOR 07/26/2017
DATEX-OHMEDA, INC. IVENT 201 07/05/2017
VYAIRE MEDICAL, INC. AVEA 06/08/2017
MAQUET CRITICAL CARE AB SERVO-I 05/24/2017
RESPIRONICS CALIFORNIA, INC ESPRIT VENTILATOR 05/08/2017
COSTA MESA MFG DC NEWPORT E500 WAVE VENTILATOR 04/25/2017
NEWPORT MEDICAL INSTRUMENTS, INC. E500 VENTILATOR 04/25/2017
RESPIRONICS CALIFORNIA, INC V200 VENTILATOR 04/05/2017
DRÄGERWERK AG & CO. KGAA EVITA V300 03/09/2017
RESPIRONICS CALIFORNIA, INC V200 VENTILATOR 03/01/2017
-
-