8 results
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41ms
·
Sources: EU EUDAMED, US FDA
Filters
FDA Adverse Event
×
AUTOSOFT 30
FDA Adverse Event
Malfunction
·UNOMEDICAL DEVICES S.A. DE C.V.·Product code FPA·May 28, 2025
INSET 30
FDA Adverse Event
Malfunction
·UNOMEDICAL DEVICES S.A. DE C.V.·Product code FPA·August 13, 2025
OT VERIO IQ METER
FDA Adverse Event
Malfunction
·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·March 19, 2013
ASR UNI FEMORAL IMPL SIZE 53
FDA Adverse Event
Injury
·DEPUY INTERNATIONAL, LTD.·Product code KWA·March 2, 2011
AXSYM DIGOXIN III
FDA Adverse Event
Malfunction
·ABBOTT DIAGNOSTICS INTERNATIONAL, LTD.·Product code KXT·May 11, 2007
Single Use Electrosurgical Knife KD-612
FDA Adverse Event
Injury
·OLYMPUS MEDICAL SYSTEMS CORP.·Product code KNS·December 15, 2021
IMPLANTABLE NEUROSTIMULATOR
FDA Adverse Event
Injury
·MEDTRONIC NEUROMODULATION·Product code MHY·December 13, 2022
CONFIDENCE SPINAL CMT SYS, 11C
FDA Adverse Event
Injury
·DEPUY SPINE INC·Product code NDN·November 3, 2021