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U.S. Department of Health and Human Services

MAUDE - Manufacturer and User Facility Device Experience

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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
 

 
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291 records meeting your search criteria returned- Product Code: FMF Product Problem: Adverse Event Without Identified Device or Use Problem Report Date From: 01/1/2016
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ManufacturerBrand NameDate Report Received
ELI LILLY AND COMPANY HUMAPEN SAVVIO 3ML (GRAY) 12/16/2019
ELI LILLY AND COMPANY HUMAPEN ERGO II 12/16/2019
MEDLINE INDUSTRIES INC. SYR W/NDLE, HYPODERM,TB,27GX 1/2", 1ML 12/05/2019
MEDLINE INDUSTRIES INC. SYR W/NDLE, SAFETY, INSLN, 1ML, 29GX0.5" 12/05/2019
MEDLINE INDUSTRIES INC. SYRSI101292-SYR W/NDLE, SAFETY, INSLN, 1 12/04/2019
ELI LILLY AND COMPANY HUMAPEN ERGO II 12/04/2019
ELI LILLY AND COMPANY HUMAPEN ERGO II 11/27/2019
ELI LILLY AND COMPANY HUMAPEN LUXURA HALF-DOSE PEN 11/27/2019
ELI LILLY AND COMPANY HUMAPEN SAVVIO 3ML (GRAY) 11/25/2019
BECTON DICKINSON MEDICAL (SINGAPORE) BD 1ML SYRINGE LUER SLIP 11/22/2019
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