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

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
 

 
 < 
 2 
 3 
 4 
 5 
 6 
 7 
 8 
 9 
 10 
 11 
 > 
 
223 records meeting your search criteria returned- Product Code: GEI Product Problem: Defective Component Report Date From: 01/1/2007

New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
GYRUS ACMI, INC G400 GENERATOR, GYRUS 12/17/2020
ARTHROCARE CORP. FA QUANTUM 2 CONTROLLER 12/08/2020
CONMED CORPORATION ABC BEND-A-BEAM 11/10/2020
LINEMASTER SWITCH CORPORATION MULTIDEBRIDER FOOTSWITCH 10/15/2020
ARTHROCARE CORP. FA QUANTUM 2 CONTROLLER 10/12/2020
ETHICON ENDO-SURGERY, INC. LAPAROSCOPIC TISSUE SEALER 09/29/2020
MEGADYNE MEDICAL PRODUCTS, INC/ ETHICON ULTRA VAC BOVIE PENCIL 09/24/2020
SMITH & NEPHEW, INC. FOOT PEDAL 09/18/2020
OLYMPUS WINTER & IBE GMBH HF UNIT "ESG-400" 09/17/2020
ARTHROCARE CORP. CII (120V) SRVC, CONTROLLER-ONLY PACKAGE 09/17/2020
-
-