72 results
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22ms
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Sources: EU EUDAMED, US FDA
Filters
Status: Malfunction
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SAIPH CEMENTED PATELLA
FDA Adverse Event
Malfunction
·MATORTHO·Product code KRP·October 24, 2025
FEMORA, TIBIAL, AND PATELLAR PROSTHESIS
FDA Adverse Event
Malfunction
·HOWMEDICA·Product code KRP·August 31, 1993
AXIAL PIN INSERTER/EXTRACTOR
FDA Adverse Event
Malfunction
·ONKOS SURGICAL·Product code KRP·January 27, 2020
ATTUNE RP TIBIAL IMPACTOR
FDA Adverse Event
Malfunction
·DEPUY IRELAND - 9616671·Product code HWA·October 8, 2018
ATTUNE RP TIBIAL IMPACTOR
FDA Adverse Event
Malfunction
·DEPUY IRELAND - 9616671·Product code HWA·October 8, 2018
ATTUNE RP PS ARTIC SURF SZ3
FDA Adverse Event
Malfunction
·DEPUY IRELAND - 9616671·Product code JWH·May 15, 2018
ATTUNE RP PS ARTIC SURF SZ3
FDA Adverse Event
Malfunction
·DEPUY IRELAND - 9616671·Product code HWT·December 9, 2020
ATTUNE FEM SIZING & FINISH
FDA Adverse Event
Malfunction
·DEPUY IRELAND - 9616671·Product code FSM·March 1, 2021
ATTUNE RP TIB BASE SZ 3 CEM
FDA Adverse Event
Malfunction
·DEPUY IRELAND - 9616671·Product code NJL·February 12, 2021
ATTUNE RP PS ARTIC SURF SZ3
FDA Adverse Event
Malfunction
·DEPUY IRELAND 9616671·Product code JWH·March 14, 2019
3ML SYRINGE 20G X 1 RP
FDA Adverse Event
Malfunction
·COVIDIEN·Product code FMF·April 3, 2019
3ML SYRINGE 20G X 1 RP
FDA Adverse Event
Malfunction
·COVIDIEN·Product code FMF·May 9, 2019
3ML SYRINGE 22G X 1 RP
FDA Adverse Event
Malfunction
·CARDINAL HEALTH·Product code FMF·March 29, 2023
3ML SYRINGE 22G X 1 RP
FDA Adverse Event
Malfunction
·CARDINAL HEALTH·Product code FMF·October 12, 2023
3ML SYRINGE 22G X 1 RP
FDA Adverse Event
Malfunction
·CARDINAL HEALTH·Product code FMF·December 16, 2022
3ML SYRINGE 22G X 1 RP
FDA Adverse Event
Malfunction
·COVIDIEN·Product code FMF·September 20, 2019
1219930ERINE CURETTE SIZE #3
FDA Adverse Event
Malfunction
·ALLEGIANCE-SURGICAL GRP·Product code HCY·April 2, 1997
ECONOMY BONE MARROW BIOPSY AND ASPIRATION TRAY
FDA Adverse Event
Malfunction
·ALLEGIANCE-SURGICAL GRP.·Product code KNW·March 24, 1997
BONE MARROW TRAY
FDA Adverse Event
Malfunction
·ALLEGIANCE-SURGICAL GRP.·Product code KNW·January 16, 1997
3000CC SUCTION LINER WITH ORTHO PORT
FDA Adverse Event
Malfunction
·ALLEGIANCE- SURGICAL GRP·Product code KDQ·January 10, 1997