9 results
·
21ms
·
Sources: EU EUDAMED, US FDA
Filters
FDA Adverse Event
×
MEDTRONIC EXTENDED
FDA Adverse Event
Malfunction
·UNOMEDICAL A/S·Product code FPA·September 27, 2024
MEDTRONIC EXTENDED
FDA Adverse Event
Malfunction
·UNOMEDICAL A/S·Product code FPA·September 27, 2024
MEDTRONIC EXTENDED
FDA Adverse Event
Malfunction
·UNOMEDICAL A/S·Product code FPA·September 27, 2024
OT VERIO IQ METER
FDA Adverse Event
Malfunction
·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·March 14, 2013
RECLAIM ASSEM UPPER PULL ROD
FDA Adverse Event
Malfunction
·DEPUY ORTHOPAEDICS, INC. 1818910·Product code LXH·August 12, 2014
DAMON COPPER NITI WIRE
FDA Adverse Event
Malfunction
·ORMCO CORPORATION·Product code DZC·February 28, 2008
SIDUS STEM-FREE SHOULDER, HUMERAL HEAD, 42-15
FDA Adverse Event
Injury
·ZIMMER GMBH·Product code HSD·June 26, 2018
SIDUS STEM-FREE SHOULDER, HUMERAL HEAD, 50-21
FDA Adverse Event
Injury
·ZIMMER GMBH·Product code HSD·June 11, 2018
NEUTRAL ELECTRODE, UNIVERSAL SIZE, WITHOUT CABLE
FDA Adverse Event
Injury
·OLYMPUS WINTER & IBE GMBH·Product code GEI·January 16, 2025