• 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
 

 
 < 
 7 
 8 
 9 
 10 
 11 
 12 
 13 
 14 
 15 
 16 
 > 
 
250 records meeting your search criteria returned- Product Code: GDW Product Problem: Unintended Ejection Report Date From: 01/1/2007

New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
ETHICON ENDO-SURGERY, LLC. GST WHITE RELOAD, 45MM, 6 ROW 09/24/2022
ETHICON ENDO-SURGERY, LLC. FLEX 60 ARTICULATING 09/24/2022
ETHICON ENDO-SURGERY, LLC. GST BLACK RELOAD, 60MM, 6 ROW 09/13/2022
ETHICON ENDO-SURGERY, LLC. ECHELON FLEX 60 COMPACT 09/06/2022
ETHICON ENDO-SURGERY, LLC. POWERED 60 ECHELON +, 340MM SHAFT 08/24/2022
ETHICON ENDO-SURGERY, LLC. POWERED PLUS STANDARD 45 08/22/2022
DAVOL INC., SUB. C.R. BARD, INC. -121364 SORBAFIX ENHANCED 08/08/2022
ETHICON ENDO-SURGERY, LLC. POWERED 60 ECHELON +, 340MM SHAFT 08/02/2022
ETHICON ENDO-SURGERY, LLC. POWERED 60 ECHELON +, 340MM SHAFT 07/29/2022
ETHICON ENDO-SURGERY, LLC. POWERED PLUS STANDARD 45 07/28/2022
-
-