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 
 8 
 9 
 10 
 > 
 
265 records meeting your search criteria returned- Product Code: MEB Product Problem: Insufficient Flow or Under Infusion Report Date From: 01/1/2009

New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
BAXTER HEALTHCARE CORPORATION INFUSOR 01/13/2021
BAXTER HEALTHCARE CORPORATION FOLFUSOR 01/05/2021
BAXTER HEALTHCARE CORPORATION INFUSOR 12/30/2020
BAXTER HEALTHCARE CORPORATION FOLFUSOR 12/16/2020
BAXTER HEALTHCARE CORPORATION FOLFUSOR 12/16/2020
BAXTER HEALTHCARE CORPORATION INFUSOR 12/02/2020
BAXTER HEALTHCARE CORPORATION INFUSOR 11/24/2020
LEVENTON S.A.U. DOSI-FUSER 11/22/2019
EPIC INTERNATIONAL (THAILAND) CO., LTD. SMARTEZ PUMP 04/08/2019
EPIC INTERNATIONAL (THAILAND) CO., LTD. SMARTEZ PUMP 02/19/2019
-
-