• 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 
 > 
 
44 records meeting your search criteria returned- Product Code: FTL Product Problem: Tear, Rip or Hole in Device Packaging Report Date From: 01/1/2016
New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
DAVOL INC., SUB. C.R. BARD, INC. -121364 MESH VENTRALEX 12/30/2020
DAVOL INC., SUB. C.R. BARD, INC. -121364 BARD FLAT MESH 12/16/2020
DAVOL INC., SUB. C.R. BARD, INC. 3DMAX 08/24/2020
DAVOL INC., SUB. C.R. BARD, INC. VENTRALIGHT ST MESH 05/14/2020
ETHICON INC. PROCEED*SURG MESH/MULTI LYR 01/27/2020
ETHICON INC. UHS MESH 10X12 11/07/2019
DAVOL INC., SUB. C.R. BARD, INC. VENTRALIGHT ST MESH 09/04/2019
ETHICON INC. ULTRAPRO HERNIA SYSTEM 06/14/2019
ETHICON INC. UHS MESH 10X12 04/04/2019
ETHICON INC. PVP SMALL 4.3CM X 4.3CM 02/15/2019
-
-