10,000 results
·
324ms
·
Sources: EU EUDAMED, US FDA
Filters
Status: Injury
×
E1 44-36 STD +3 HMRL BRG
FDA Adverse Event
Injury
·BIOMET SET·Product code PAO·September 29, 2015
COMP RVRS SHLDR GLNSP STD 36MM
FDA Adverse Event
Injury
·BIOMET SET·Product code PAO·September 29, 2015
COMP PRIMARY STEM 8MM MINI
FDA Adverse Event
Injury
·BIOMET SET·Product code KWS·September 28, 2015
HOSPIRA . ICU MEDICAL
FDA Adverse Event
Injury
·SET SOURCE·Product code FPA·August 10, 2012
HOSPIRA / ICU MEDICAL
FDA Adverse Event
Injury
·SET SOURCE·Product code FPA·August 10, 2012
HOSPIRA / ICU MEDICAL
FDA Adverse Event
Injury
·SET SOURCE·Product code FPA·August 10, 2012
HOSPIRA / ICU MEDICAL
FDA Adverse Event
Injury
·SET SOURCE·Product code FPA·August 10, 2012
HOSPIRA / ICU MEDICAL
FDA Adverse Event
Injury
·SET SOURCE·Product code FPA·August 10, 2012
EXPLOR 7X26MM IMPL STEM W/SCR
FDA Adverse Event
Injury
·BIOMET SET·Product code KWI·September 28, 2015
COMP RVS GLENS 2 PRONG INS/IMP
FDA Adverse Event
Injury
·BIOMET SET·Product code LXH·October 16, 2015
COMP CNV GLEN LINER IMPACTOR
FDA Adverse Event
Injury
·BIOMET SET·Product code KWS·October 8, 2015
SMITHS MEDICAL
FDA Adverse Event
Injury
·CADD EXTENSION SET·Product code FPA·April 21, 2014
*
FDA Adverse Event
Injury
·HORIZON PUMP IV SET·Product code FPA·April 10, 2003
SET SOURCE SECONDARY TUBING WITH ATTACHED CLOSED MALE ADAPTO
FDA Adverse Event
Injury
·ICU/SPIROS/SET SOURCE·Product code FPA·March 3, 2008
QUICK SET
FDA Adverse Event
Injury
·MEDTRONIC QUICK SET - UNI MEDICAL·Product code FPA·July 10, 2012
KIM MED TECH INC.
FDA Adverse Event
Injury
·KIM ENDOSCOPIC NASAL INTESTIONAL TUBE SET·Product code FEG·June 1, 1992
SET, ADMINISTRATION, FOR PERITONEAL DIALYSIS, DISPOSABLE
FDA Adverse Event
Injury
·BAXTER HEALTHCARE SET, ADMINISTRATION, FOR PERITON·Product code KDJ·May 25, 2011
QUICK-SET INFUSION SET
FDA Adverse Event
Injury
·MEDTRONIC MINIMED·Product code FPA·November 14, 2016
QUICK SET INFUSION SET
FDA Adverse Event
Injury
·MEDTRONIC·Product code FRN·September 22, 2017
SOF-SET IV SET
FDA Adverse Event
Injury
·MINIMED TECHNOLOGIES·Product code FOZ·January 30, 1996