6 results
·
36ms
·
Sources: EU EUDAMED, US FDA
Filters
Status: Malfunction
×
MYOMEN INSTRUMENT
FDA Adverse Event
Malfunction
·KARL STORZ SE & CO. KG·Product code HET·September 2, 2025
BLOOD GLOUSE MONITOR
FDA Adverse Event
Malfunction
·ABBOTT DIABETES CARE INC.·Product code QBJ·December 9, 2025
BLOOD GLOUSE MONITOR
FDA Adverse Event
Malfunction
·ABBOTT DIABETES CARE, INC.·Product code QBJ·December 9, 2025
BD PLASTIPAK 50ML CONCENTRIC LUER LOCK SYRINGE
FDA Adverse Event
Malfunction
·BECTON DICKINSON, S.A.·Product code FMF·November 6, 2019
BD LUER-LOK¿ SYRINGE WITH ATTACHED NEEDLE 25 G X 1 IN
FDA Adverse Event
Malfunction
·BECTON DICKINSON MEDICAL SYSTEMS·Product code FMF·September 1, 2022
CAPSURE Z NOVUS
FDA Adverse Event
Malfunction
·MPRI·Product code DTB·August 9, 2013