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

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 
 6 
 7 
 8 
 9 
 10 
 > 
 
97 records meeting your search criteria returned- Product Code: FSA Product Problem: Device Handling Problem Report Date From: 01/1/2007
New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
MEDIBO MEDICAL PRODUCTS NV SARA 3000 04/04/2023
LIKO AB LIKORALL 242 S, NATURAL 03/17/2023
HANDI-MOVE NV HANDI-MOVE - 2510 CEILING MOTOR 12/06/2022
LIKO AB LIKORALL 200 10/19/2022
ARJOHUNTLEIGH MAGOG INC. MAXI MOVE 01/14/2022
ARJOHUNTLEIGH MAGOG INC. MAXI MOVE 12/21/2021
ARJOHUNTLEIGH MAGOG INC. MAXI MOVE 08/05/2021
ARJOHUNTLEIGH MAGOG INC. MAXI MOVE 08/05/2021
ARJO DOMINICAN REPUBLIC SLINGS, LOOP 09/03/2019
ARJO HOSPITAL EQUIPMENT AB CONCERTO + BASIC 08/01/2019
-
-