10 results
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20ms
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Sources: EU EUDAMED, US FDA
Filters
FDA Adverse Event
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BD VACUTAINER PPT PLASMA PREPARATION TUBE K2E 9.0 MG
FDA Adverse Event
Malfunction
·BECTON, DICKINSON & CO.·Product code JKA·May 7, 2018
BD VACUTAINER® PPT¿ PLASMA PREPARATION TUBE K2E 9.0 MG
FDA Adverse Event
Malfunction
·BECTON, DICKINSON & CO.·Product code JKA·April 26, 2018
BD VACUTAINER® PPT¿ PLASMA PREPARATION TUBE K2E 9.0 MG
FDA Adverse Event
Malfunction
·BECTON, DICKINSON & CO.·Product code JKA·April 26, 2018
BD VACUTAINER® PPT¿ PLASMA PREPARATION TUBE K2E 9.0 MG
FDA Adverse Event
Malfunction
·BECTON, DICKINSON & CO.·Product code JKA·April 26, 2018
TPRLC 133 MP TYPE1 PPS HO 16.0
FDA Adverse Event
Malfunction
·ZIMMER BIOMET, INC.·Product code KWA·February 24, 2022
8F X 18CM HEMO-CATH
FDA Adverse Event
Malfunction
·MEDCOMP·Product code MSD·February 15, 2013
PRECISION XTRA
FDA Adverse Event
Malfunction
·Product code NBW·January 27, 2011
G4 PLATINUM CONTINUOUS GLUCOSE MONITORING SYSTEM
FDA Adverse Event
Malfunction
·DEXCOM, INC.·Product code MDS·July 31, 2014
LOGIC TIBIA PS MOD INSRT SZ 3 9MM
FDA Adverse Event
Injury
·EXACTECH, INC.·Product code JWH·November 11, 2024
BD VACUTAINER® PPT¿ PLASMA PREPARATION TUBE K2E 9.0 MG
FDA Adverse Event
Malfunction
·BECTON, DICKINSON & CO.·Product code JKA·July 17, 2018