7 results
·
28ms
·
Sources: EU EUDAMED, US FDA
Filters
FDA Adverse Event
×
ACCU-CHEK SPIRIT
FDA Adverse Event
Injury
·ROCHE INSULIN DELIVERY SYSTEMS INC.·Product code LZG·June 18, 2010
SPECTRUM INFUSION PUMP
FDA Adverse Event
Malfunction
·BAXTER HLTHACARE CORP·Product code FRN·February 7, 2014
PRECISE PRO RX CAROTID STENT SYSTEM
FDA Adverse Event
Injury
·CORDIS DE MEXICO·Product code NIM·December 21, 2012
BIOLOX DELTA CER OPTION TYPE 1 TPR SLEVE -3
FDA Adverse Event
Injury
·BIOMET UK LTD.·Product code LZO·August 19, 2025
TRILOGY
FDA Adverse Event
Injury
·ZIMMER BIOMET, INC.·Product code LPH·August 14, 2025
BIOLOX DELTA CER OPTION HD 28MM
FDA Adverse Event
Injury
·BIOMET UK LTD.·Product code LZO·August 19, 2025
DUAL MOBILITY VIVACIT E
FDA Adverse Event
Injury
·ZIMMER BIOMET, INC.·Product code LPH·August 14, 2025