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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
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284 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 ERGO II 10/01/2020
ELI LILLY AND COMPANY HUMAPEN ERGO II 10/01/2020
BECTON DICKINSON UNSPECIFIED BD POSIFLUSH SYRINGE 09/21/2020
BECTON DICKINSON UNSPECIFIED BD POSIFLUSH SYRINGE 09/01/2020
BECTON, DICKINSON AND CO. BD POSIFLUSH XS PRE-FILLED FLUSH SYRINGE 08/27/2020
BECTON DICKINSON UNSPECIFIED BD POSIFLUSH SYRINGE 08/26/2020
BD MEDICAL (BD WEST) MEDICAL SURGICAL SYRINGE 10ML POSIFLUSH LA 08/20/2020
ELI LILLY AND COMPANY HUMAPEN, UNKNOWN DEVICE 08/12/2020
ELI LILLY AND COMPANY HUMAPEN UNKNOWN DEVICE 07/24/2020
ELI LILLY AND COMPANY HUMAPEN ERGO II 07/24/2020
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