11 results
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17ms
·
Sources: EU EUDAMED, US FDA
Filters
Status: Malfunction
×
SURELIFE ARM BP MONITOR-PREMIUM
FDA Adverse Event
Malfunction
·MHC MEDICAL PRODUCTS, LLC·Product code DXN·June 19, 2018
VENTED AUTOFEED HUMIDIFICATION CHAMBER
FDA Adverse Event
Malfunction
·Product code BTT·July 29, 2020
PROLIEVE THERMODILITATION KIT
FDA Adverse Event
Malfunction
·BOSTON SCIENTIFIC CORPORATION·Product code MEQ·October 15, 2008
COLLEAGUE PRE P1.7
FDA Adverse Event
Malfunction
·BAXTER HEALTHCARE - SINGAPORE·Product code FRN·August 10, 2011
MINICAP
FDA Adverse Event
Malfunction
·BAXTER HEALTHCARE - CLEVELAND·Product code KDI·July 1, 2013
ANIMAS INSULIN CARTRIDGE
FDA Adverse Event
Malfunction
·ANIMAS CORPORATION·Product code LZG·April 29, 2016
PROXIMAL HUMERUS, LEFT, ÿ 7X160MM
FDA Adverse Event
Malfunction
·ZIMMER GMBH·Product code HSB·October 8, 2024
NEEDLE 25GA 5/8IN
FDA Adverse Event
Malfunction
·BECTON DICKINSON, S.A.·Product code FMI·December 7, 2020
MINICOLLECT TUBE 0.5 ML K2E K2EDTA LAVENDER CAP, WITH CROSS CUT, SPRAY-DRIED
FDA Adverse Event
Malfunction
·GREINER BIO-ONE GMBH·Product code JKA·August 28, 2020
NEEDLE 25GA 5/8IN
FDA Adverse Event
Malfunction
·BECTON DICKINSON, S.A.·Product code FMI·January 15, 2021
ONE TOUCH ULTRALINK METER
FDA Adverse Event
Malfunction
·LIFESCAN, INC.·Product code NBW·September 4, 2009