7 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® K2E (EDTA) 18.0MG PLUS BLOOD COLLECTION TUBES
FDA Adverse Event
Malfunction
·BECTON, DICKINSON AND COMPANY (BD)·Product code JKA·June 20, 2024
NCB PERIPROSTHETIC FEMUR POLYAXIAL LOCKING PLATE SYSTEM
FDA Adverse Event
Injury
·ZIMMER, INC.·Product code HRS·April 4, 2023
BD VACUTAINER® K2E (EDTA) 18.0MG PLUS BLOOD COLLECTION TUBES
FDA Adverse Event
Malfunction
·BECTON, DICKINSON AND COMPANY (BD)·Product code JKA·March 25, 2024
MINILINK TRANSMITTER
FDA Adverse Event
Malfunction
·MEDTRONIC MINIMED·Product code MDS·October 14, 2014
42" FLOOR LOADER
FDA Adverse Event
STERIS MEXICO, S. DE R.L. DE C.V.·Product code FLE·June 14, 2013
NAVIGATION SOFTWARE 1.6.3 SMITH & NEPHEW
FDA Adverse Event
Other
·BRAINLAB AG·Product code HAW·June 20, 2011
NSK
FDA Adverse Event
Injury
·NAKANISHI INC.·Product code EGS·January 30, 2017