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 
 > 
 
37 records meeting your search criteria returned- Product Code: JOH Product Problem: Device Dislodged or Dislocated Report Date From: 01/1/2007

New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
SMITHS MEDICAL INTERNATIONAL, LTD. PORTEX 12/19/2020
SMITHS MEDICAL ASD, INC. BIVONA 08/13/2020
SMITHS MEDICAL ASD, INC. PORTEX BIVONA FLEXTEND TTS PEDIATRIC STR 10/10/2019
SMITHS MEDICAL ASD, INC. PORTEX BIVONA FLEXTEND TTS PEDIATRIC STR 10/10/2019
SMITHS MEDICAL ASD, INC. PORTEX BIVONA FLEXTEND TTS PEDIATRIC STR 10/10/2019
SMITHS MEDICAL ASD, INC. PORTEX® PORTEX® BLUE LINE ULTRA® CUFFED 08/19/2019
COVIDIEN SHILEY 09/12/2018
MMJ SA DE CV(USD) SHILEY 08/07/2018
COVIDIEN LLC SHILEY¿ EVAC ENDOTRACHEAL 07/06/2018
SMITHS MEDICAL, ASD, INC. PORTEX® CUFFED BLUE LINE ULTRA® TRACHEOS 04/24/2018
-
-