6 results
·
21ms
·
Sources: EU EUDAMED, US FDA
Filters
FDA Adverse Event
×
BD PLASTIPAK¿ LUER-LOCK SYRINGE
FDA Adverse Event
Malfunction
·BECTON DICKINSON, S.A.·Product code FMF·June 25, 2018
PROFEMUR(R) COCR NECK
FDA Adverse Event
Injury
·MICROPORT ORTHOPEDICS INC.·Product code KWA·May 9, 2014
FREESTYLE FLASH
FDA Adverse Event
Malfunction
·ABBOTT DIABETES CARE INC, USA·Product code LFR·October 5, 2007
MECHANICAL WALKER, ROLLATOR
FDA Adverse Event
SHUNLONG PHYSICAL THERAPY EQUIPMENT·Product code ITJ·October 23, 2012
ESSURE
FDA Adverse Event
Injury
·BAYER PHARMA AG·Product code HHS·October 23, 2018
SYRINGE 30ML LL BNS
FDA Adverse Event
Malfunction
·BECTON DICKINSON AND COMPANY·Product code FMF·September 20, 2019