• 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 
 > 
 
36 records meeting your search criteria returned- Product Code: FMF Product Problem: Device Fell Report Date From: 01/1/2016
New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
IMS LIMITED MORPHINE SULFATE INJECTION, USP 09/16/2021
ELI LILLY AND COMPANY HUMAPEN ERGO II 06/23/2021
ELI LILLY AND COMPANY, PHARMACEUTICAL DE KWIK PEN 05/25/2021
ELI LILLY AND COMPANY HUMAPEN ERGO II 05/21/2021
ELI LILLY AND COMPANY HUMAPEN ERGO II 05/21/2021
ELI LILLY AND COMPANY HUMAPEN LUXURA HALF-DOSE PEN 04/23/2021
ALLISON MEDICAL, INC. SAFETY FIRST LUER LOCK 1 ML 23 GAUGE/1 I 04/13/2021
ALLISON MEDICAL, INC. SAFETY FIRST LUER LOCK 1 ML 23 GAUGE/1 I 04/13/2021
ALLISON MEDICAL, INC. SAFETY FIRST LUER LOCK 1 ML 23 GAUGE/1 I 04/13/2021
ELI LILLY AND COMPANY HUMAPEN LUXURA HALF-DOSE PEN 04/05/2021
-
-