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U.S. Department of Health and Human Services

Manufacturer and User Facility Device Experience (MAUDE)
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135 records meeting your search criteria returned- Product Code: FMG Product Problem: Device Contamination with Chemical or Other Material Report Date From: 01/1/2009

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ManufacturerBrand NameDate Report Received
BD INFUSION THERAPY SYSTEMS INC. S.A. DE CONNECTA PLUS3 WHITE BLEND 09/30/2020
BD INFUSION THERAPY SYSTEMS INC. S.A. DE CONNECTA PLUS3 WHITE BLEND 09/17/2020
BD INFUSION THERAPY SYSTEMS INC. S.A. DE CONNECTA PLUS3 10CM WHITE 06/25/2020
BD INFUSION THERAPY SYSTEMS INC. S.A. DE BD CONNECTA 3-WAY STOPCOCK 06/08/2020
BD INFUSION THERAPY SYSTEMS INC. S.A. DE CONNECTA Q-SYTES WHT 05/19/2020
BD INFUSION THERAPY SYSTEMS INC. S.A. DE STPCK Q-SYTE WHT 360DEG W/O NUT CAP NS 03/09/2020
BD INFUSION THERAPY SYSTEMS INC. S.A. DE CONNECTA PLUS1 360 WHITE BLEND 03/09/2020
BD INFUSION THERAPY SYSTEMS INC. S.A. DE STPCK Q-SYTE WHT 360DEG W/O NUT CAP NS 03/09/2020
BD INFUSION THERAPY SYSTEMS INC. S.A. DE STOPCOCK Q-SYTE WHT 360DEG NONSTERILE 03/09/2020
BD INFUSION THERAPY SYSTEMS INC. S.A. DE STOPCOCK Q-SYTE WHT 360DEG NONSTERILE 03/09/2020
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