9 results
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28ms
·
Sources: EU EUDAMED, US FDA
Filters
FDA Adverse Event
×
MINIMED QUICK-SET
FDA Adverse Event
Injury
·UNOMEDICAL A/S·Product code FPA·May 30, 2025
MINIMED QUICK-SET
FDA Adverse Event
Injury
·UNOMEDICAL DEVICES S.A. DE C.V.·Product code FPA·June 19, 2025
MINIMED QUICK-SET
FDA Adverse Event
Malfunction
·UNOMEDICAL DEVICES S.A. DE C.V.·Product code FPA·July 8, 2025
MINIMED QUICK-SET
FDA Adverse Event
Malfunction
·UNOMEDICAL DEVICES S.A. DE C.V.·Product code FPA·April 8, 2025
AXSYM DIGOXIN III
FDA Adverse Event
Malfunction
·ABBOTT DIAGNOSTICS INTERNATIONAL, LTD.·Product code KXT·May 11, 2007
OT ULTRALINK METER
FDA Adverse Event
Malfunction
·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·March 19, 2013
TOTAL CARE
FDA Adverse Event
Malfunction
·HILL-ROM, INC.·Product code FNL·March 2, 2011
BD PLASTIPAK 20ML SYRINGE LUER-LOK
FDA Adverse Event
Malfunction
·BECTON DICKINSON, S.A.·Product code FMF·March 11, 2021
MEDTRONIC NAVIGATION
FDA Adverse Event
Injury
·MEDTRONIC NAVIGATION, INC·Product code HAW·March 1, 2024