• 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
 

 
 < 
 4 
 5 
 6 
 7 
 8 
 9 
 10 
 > 
 
100 records meeting your search criteria returned- Product Code: BZD Product Problem: Device Contamination with Chemical or Other Material Report Date From: 01/1/2019

New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
PHILIPS / RESPIRONICS, INC. DREAMSTATION 09/20/2021
PHILIPS / RESPIRONICS, INC. RESPIRONICS DREAMSTATION CPAP 09/15/2021
PHILIPS / RESPIRONICS, INC. DREAMSTATION AUTO CPAP 08/27/2021
PHILIPS / RESPIRONICS, INC. DREAMSTATION AUTO CPAP 08/26/2021
PHILIPS / RESPIRONICS, INC. DREAMSTATION 08/23/2021
PHILIPS / RESPIRONICS INC. DREAMSTATION CPAP, AUTO CPAP, BIPAP 08/17/2021
PHILIPS RESPIRONICS, INC. DREAM MACHINE CPAP 08/17/2021
PHILIPS / RESPIRONICS, INC. DREAMSTATION 08/17/2021
PHILIPS / RESPIRONICS, INC. PHILLIPS RESPIRONICS REMSTAR AUTO DOM 08/09/2021
RESPIRONICS, INC. REMSTAR AUTO A-FLEX, SYS ONE, 60 SRS,DOM 08/05/2021
-
-