22 results
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21ms
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Sources: EU EUDAMED, US FDA
Filters
Status: Injury
×
TRANSVENE
FDA Adverse Event
Injury
·RICE CREEK MFG·Product code LWS·February 11, 2013
TENDRIL ST
FDA Adverse Event
Injury
·ST JUDE MEDICAL CARDIAC RHYTHM MANAGEMENT DIVISION·Product code DTB·January 10, 2011
UNI GLENOID-PERIPHERAL LOCK SCRW
FDA Adverse Event
Injury
·ARTHREX, INC.·Product code PHX·October 28, 2020
UNIVERSAL GLENOID - CENTRAL SCREW 15MM
FDA Adverse Event
Injury
·ARTHREX, INC.·Product code PHX·October 28, 2020
UNIVERS REVERS SPACER 36+15MM
FDA Adverse Event
Injury
·ARTHREX, INC.·Product code PHX·October 28, 2020
UNIVERS REVERS GLENO 36 +4 LAT
FDA Adverse Event
Injury
·ARTHREX, INC.·Product code PHX·October 28, 2020
UNI GLENOID-PERIPHERAL LOCK SCRW
FDA Adverse Event
Injury
·ARTHREX, INC.·Product code PHX·October 28, 2020
UNIVERS REVERS STEM, SIZE 7, CAP COATED
FDA Adverse Event
Injury
·ARTHREX, INC.·Product code KWS·October 28, 2020
FW,BPB #2 SUTR,BLU W/NDL
FDA Adverse Event
Injury
·ARTHREX, INC.·Product code GAT·October 28, 2020
#5 FIBERWIRE W/ NEEDLES FOR SUTUREPLATE
FDA Adverse Event
Injury
·ARTHREX, INC.·Product code GAT·October 28, 2020
UNIVERS REVS CUP,36/NEUTRAL CTD
FDA Adverse Event
Injury
·ARTHREX, INC.·Product code PHX·October 28, 2020
UNIVERSAL GLENOID - BASEPLATE SMALL
FDA Adverse Event
Injury
·ARTHREX, INC.·Product code PHX·October 28, 2020
HUMERAL INSERT S/36 +3 TO FIT IN 36 CUP
FDA Adverse Event
Injury
·ARTHREX, INC.·Product code PHX·October 28, 2020
UNK
FDA Adverse Event
Injury
·ARTHREX, INC.·Product code PHX·September 19, 2024
UNK
FDA Adverse Event
Injury
·ARTHREX, INC.·Product code PHX·September 19, 2024
UNK
FDA Adverse Event
Injury
·ARTHREX, INC.·Product code PHX·September 19, 2024
UNIVERS REVERS HUMERAL STEM, SIZE 9
FDA Adverse Event
Injury
·ARTHREX, INC.·Product code HSD·June 25, 2024
UNIVERS REVERS FRACTURE ADAPTER TRUNION
FDA Adverse Event
Injury
·ARTHREX, INC.·Product code HSD·June 25, 2024
FRACTURE ADAPTER, SZ 6-9, WIDE + TALL
FDA Adverse Event
Injury
·ARTHREX, INC.·Product code HSD·May 30, 2024
REVERS CA HUMERAL HEAD, 56/22
FDA Adverse Event
Injury
·ARTHREX, INC.·Product code HSD·June 25, 2024