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 
 3 
 4 
 5 
 6 
 7 
 8 
 9 
 10 
 > 
 
111 records meeting your search criteria returned- Product Code: DTZ Product Problem: Device Damaged Prior to Use Report Date From: 01/1/2009
New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
TERUMO MEDICAL CORPORATION CAPIOX FX15 OXYGENATOR 12/27/2023
TERUMO MEDICAL CORPORATION CAPIOX FX25 OXYGENATOR 12/27/2023
TERUMO CORPORATION, ASHITAKA CAPIOX FX OXYGENATOR 04/28/2022
TERUMO CARDIOVASCULAR SYSTEMS CORPORATIO STERILE FX25RWC W/ RES 10/19/2021
TERUMO CARDIOVASCULAR SYSTEMS CORPORATIO STERILE FX25REC W/RES 04/23/2021
TERUMO CARDIOVASCULAR SYSTEMS CORPORATIO STERILE FX25REC W/RES 02/26/2021
TERUMO CARDIOVASCULAR SYSTEMS CORPORATIO STERILE FX25REC W/RES 01/12/2021
TERUMO CARDIOVASCULAR SYSTEMS CORPORATIO CAPIOX RX25 OXYGENATOR EAST 08/24/2020
TERUMO CARDIOVASCULAR SYSTEMS CORPORATIO STERILE FX15RWC W/ 4L RES 06/12/2020
TERUMO CARDIOVASCULAR SYSTEMS CORPORATIO STERILE FX25REC W/RES 12/13/2019
-
-