8 results
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21ms
·
Sources: EU EUDAMED, US FDA
Filters
FDA Adverse Event
×
TUFF UNICON IMPLANT
FDA Adverse Event
Injury
·NORIS MEDICAL LTD·Product code DZE·March 25, 2026
GOBED II
FDA Adverse Event
Malfunction
·STRYKER MEDICAL-KALAMAZOO·Product code FNL·March 13, 2013
GEMSTAR 7 THERAPY
FDA Adverse Event
Malfunction
·HOSPIRA, INC·Product code FRN·January 26, 2011
LIFESYNC ECG SYSTEM
FDA Adverse Event
Death
·LIFESYNC CORPORATION·Product code DRT·February 21, 2008
UNKNOWN RIGIDFIX CROSS PIN
FDA Adverse Event
Injury
·DEPUY MITEK LLC US·Product code HTY·July 29, 2019
UNK - GUIDES/SLEEVES - RIGIDFIX
FDA Adverse Event
Injury
·DEPUY MITEK LLC US·Product code LXH·July 29, 2019
UNKNOWN BIO-INTRAFIX
FDA Adverse Event
Injury
·DEPUY MITEK LLC US·Product code HWC·July 29, 2019
BACFIX ROD, UNKNOWN
FDA Adverse Event
Injury
·ZIMMER BIOMET SPINE INC.·Product code HSB·January 16, 2020