72 results · 22ms · Sources: EU EUDAMED, US FDA

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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