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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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41 records meeting your search criteria returned- Product Code: FMI Product Problem: Improper Flow or Infusion Report Date From: 01/1/2009

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ManufacturerBrand NameDate Report Received
HTL-STREFA S.A. DROPLET PEN NEEDLE 08/20/2021
HTL-STREFA S.A. TRUEPLUS, STERILE PEN NEEDLES 08/20/2021
HTL-STREFA S.A. TRUEPLUS, STERILE PEN NEEDLES 08/19/2021
HTL-STREFA S.A. DROPLET PEN NEEDLE 08/19/2021
MHC MEDICAL PRODUCTS, LLC. EASYTOUCH 02/04/2020
MHC MEDICAL PRODUCTS, LLC. EASYTOUCH 10/25/2019
MHC MEDICAL PRODUCTS, LLC. EASYTOUCH 10/25/2019
TRIVIDIA HEALTH, INC PEN NEEDLES FG 09/25/2019
TELEFLEX MEDICAL ARROW EZ IO NEEDLE SET 08/23/2019
HTL-STREFA S.A. DROPLET 07/19/2019
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