• 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 
 > 
 
172 records meeting your search criteria returned- Product Code: FPA Product Problem: Tear, Rip or Hole in Device Packaging Report Date From: 01/1/2019

New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
C.R. BARD, INC. (BASD) -3006260740 POWERLOC SAFETY INFUSION SET 20G X 0.75I 12/05/2023
C.R. BARD, INC. (BASD) -3006260740 POWERLOC SAFETY INFUSION SET 20G X 0.75I 07/29/2023
C.R. BARD, INC. (BASD) -3006260740 POWERLOC SAFETY INFUSION SET 20G X 0.75I 07/12/2023
C.R. BARD, INC. (BASD) -3006260740 POWERLOC SAFETY INFUSION SET 20G X 0.75I 06/14/2023
BAXTER HEALTHCARE CORPORATION CLEARLINK LUER ACTIVATED VALVE 06/14/2023
C.R. BARD, INC. (BASD) -3006260740 POWERLOC SAFETY INFUSION SET 20G X 0.75I 05/31/2023
CAREFUSION 303, INC. ALARIS, SMARTSITE 04/19/2023
BAXTER HEALTHCARE CORPORATION SOLUTION ADMINISTRATION SETS 03/31/2023
CAREFUSION 303, INC. ALARIS, SMARTSITE 03/24/2023
BAXTER HEALTHCARE CORPORATION EXTENSION SETS WITH ONE-LINK NEEDLE-FREE 03/16/2023
-
-