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
 

 
 < 
 1 
 2 
 3 
 4 
 5 
 6 
 7 
 > 
 
65 records meeting your search criteria returned- Product Code: FTL Product Problem: Improper or Incorrect Procedure or Method Report Date From: 01/1/2007

New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
ETHICON INC. PROLENE* POLYPROPYLENE MESH 05/11/2018
ATRIUM MEDICAL CORP. PROLOOP 10/11/2017
COOK BIOTECH ¿ZENAPRO HYBRID HERNIA REPAIR GRAFT 06/29/2017
Unknown Manufacturer MESH 04/19/2017
Unknown Manufacturer HERNIA SURGICAL MESS IMPLANT 08/18/2016
Unknown Manufacturer LUNG-VICRBRACHY TYL MESH SUTURE INTERST 02/09/2016
ETHICON INC. PHYSIOMESH HERNIA MESH 01/02/2016
DAVOL INC., SUBSIDIARY OF CR BARD INC. VENTRALIGHT ST MESH WITH ECHO PS POSITIO 12/29/2015
ETHICON PROLEEN 10/07/2015
TEI BIOSCIENCES INC. PRIMATRIX AG 06/23/2015
-
-