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U.S. Department of Health and Human Services

Manufacturer and User Facility Device Experience (MAUDE)

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Super Search Devices@FDA
510(k) | DeNovo | Registration & Listing | Adverse Events | Recalls | PMA | HDE | Classification | Standards
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85 records meeting your search criteria returned- Product Code: FMI Patient Problem: Underdose Report Date From: 01/1/2009

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ManufacturerBrand NameDate Report Received
BECTON DICKINSON UNSPECIFIED BD¿ PEN NEEDLE 07/10/2019
BECTON DICKINSON UNSPECIFIED BD¿ PEN NEEDLE 07/09/2019
BECTON DICKINSON PEN II OMNITROPE PEN 10 07/01/2019
BECTON DICKINSON PEN II OMNITROPE PEN 10 05/30/2019
BECTON DICKINSON AND CO. BD ULTRA FINE¿ PEN NEEDLES 05/22/2019
BECTON DICKINSON UNSPECIFIED BD¿ PEN NEEDLE 05/17/2019
BECTON DICKINSON ORGANON FOLLISTIM PEN 2ND GEN PEN II 05/09/2019
BECTON DICKINSON AND CO. BD ULTRA FINE¿ PEN NEEDLE 04/15/2019
BECTON DICKINSON PEN II MYLAN 3.0ML 03/27/2019
BECTON DICKINSON ORGANON FOLLISTIM PEN® 2ND GEN PEN II 03/26/2019
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