6 results
·
27ms
·
Sources: EU EUDAMED, US FDA
Filters
FDA Adverse Event
×
BACT/ALERT® FN PLUS
FDA Adverse Event
Malfunction
·BIOMERIEUX INC.·Product code MDB·August 17, 2019
NONE - SEE PHYSICIAN COMMENTS IN H10.
FDA Adverse Event
Injury
·Product code JWH·October 16, 2013
RETROFLEX3 INTRODUCER SHEATH
FDA Adverse Event
Injury
·EDWARDS LIFESCIENCES·Product code DYB·April 11, 2013
FLO-GARD 6201 VOLUMETRIC INFUSION PUMP
FDA Adverse Event
Malfunction
·BAXTER HEALTHCARE (SG)·Product code FRN·May 27, 2008
ACUITY
FDA Adverse Event
Injury
·CPI - DEL CARIBE·Product code OJX·April 13, 2011
SPIRAL BLADE F/EXPERT RFN L75 TAN GOLD
FDA Adverse Event
Injury
·WRIGHTS LANE: SYNTHES USA PRODUCTS LLC·Product code HSB·January 9, 2018