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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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488 records meeting your search criteria returned- Product Code: FPA Product Problem: Adverse Event Without Identified Device or Use Problem Report Date From: 01/1/2016
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ManufacturerBrand NameDate Report Received
REPRO-MED SYSTEMS, INC. DBA KORU MEDICAL RMS4-2609 HIGH FLO NEEDLE SETS 03/16/2021
SMITHS MEDICAL ASD, INC. CLEO INFUSION SET 03/12/2021
SMITHS MEDICAL ASD, INC. CLEO INFUSION SET 03/12/2021
SMITHS MEDICAL ASD, INC. CADD EXT SET 02/23/2021
BECTON DICKINSON UNSPECIFIED BD CONNECTA 02/22/2021
BECTON DICKINSON UNSPECIFIED BD CONNECTA 02/22/2021
BECTON DICKINSON UNSPECIFIED BD CONNECTA 02/19/2021
BECTON DICKINSON UNSPECIFIED BD Q-SYTE 02/19/2021
ROCHE DIABETES CARE, INC. ACCU-CHEK FLEXLINK INFUSION SET 02/18/2021
Unknown Manufacturer MIO 02/17/2021
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