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 
 
 
29 records meeting your search criteria returned- Product Code: MCW Product Problem: Device Markings/Labelling Problem Report Date From: 01/1/2019

New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
UNKNOWN ROTAREX 05/31/2022
UNKNOWN ROTAREX 05/31/2022
UNKNOWN ROTAREX 05/25/2022
UNKNOWN ROTAREX 03/30/2022
CARDIOVASCULAR SYSTEMS INCORPORATED VIPERSLIDE 03/08/2022
UNKNOWN IV BAG 03/08/2022
UNKNOWN ROTAREX 12/09/2021
EXIMO MEDICAL LTD. CATHETER EXIMO ATHERECTOMY 12/28/2020
CARDIOVASCULAR SYSTMS, INC. VIPERSLIDE IV BAG 100 ML 01/08/2019
-
-