645 results
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37ms
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Sources: EU EUDAMED, US FDA
Filters
Status: Malfunction
×
REN - HARDWARE
FDA Adverse Event
Malfunction
·BAXTER HEALTHCARE - LARGO·Product code FKX·February 19, 2011
ULTRACISION SURG DEV, CURVED SHEARS, ENDO
FDA Adverse Event
Malfunction
·ETHICON ENDO SURGERY, INC.(CINCINNATI)·Product code LFL·July 11, 2005
INFINITI VISION SYSTEM
FDA Adverse Event
Malfunction
·ALCON - IRVINE TECHNOLOGY CENTER·Product code HQC·May 12, 2006
PARIETEX
FDA Adverse Event
Malfunction
·SOFRADIM PRODUCTION SAS·Product code FTL·April 11, 2025
HEARTMATE CORING KNIFE
FDA Adverse Event
Malfunction
·THORATEC CORP.·Product code DSQ·July 20, 2004
UNKNOWN ABSORBATACK
FDA Adverse Event
Malfunction
·COVIDIEN LP LLC NORTH HAVEN·Product code GDW·April 11, 2025
PRECISION IDEAL EYES 5.5MM 30°, HD AUTOCLAVABLE LAPAROSCOPE 30CM
FDA Adverse Event
Malfunction
·STRYKER ENDOSCOPY-SAN JOSE·Product code GCJ·December 15, 2022
KYPHX HV-R BONE CEMENT
FDA Adverse Event
Malfunction
·MEDTRONIC SPINE LLC·Product code NDN·February 10, 2010
DIALYSIS UNKNOWN
FDA Adverse Event
Malfunction
·COVIDIEN MFG SOLUTIONS S.A.·Product code FJS·July 28, 2020
DIALYSIS UNKNOWN
FDA Adverse Event
Malfunction
·COVIDIEN MFG SOLUTIONS S.A.·Product code FJS·July 28, 2020
HARMONIC SCALPEL CURVED SHEAR
FDA Adverse Event
Malfunction
·ETHICON ENDO SURGERY, INC.(CINCINNATI)·Product code LFL·November 3, 2006
ENDOPATH DILATING TIP TROCAR
FDA Adverse Event
Malfunction
·ETHICON ENDO-SURGERY, INC.·Product code GCJ·December 23, 1997
KYPHX HV-R BONE CEMENT
FDA Adverse Event
Malfunction
·MEDTRONIC SPINE LLC·Product code NDN·February 10, 2010
CEMENT, BONE, VERTEBROPLASTY
FDA Adverse Event
Malfunction
·MEDTRONIC SOFAMOR DANEK·Product code NDN·June 9, 2015
CEMENT, BONE, VERTEBROPLASTY
FDA Adverse Event
Malfunction
·MEDTRONIC SOFAMAR DANEK·Product code NDN·June 9, 2015
CEMENT, BONE, VERTEBROPLASTY
FDA Adverse Event
Malfunction
·MEDTRONIC SOFAMOR DANEK·Product code NDN·June 9, 2015
QUANTUM TTC BILIARY BALLOON DILATOR
FDA Adverse Event
Malfunction
·COOK ENDOSCOPY·Product code FGE·April 13, 2022
UNKNOWN HIP FEMORAL HEAD
FDA Adverse Event
Malfunction
·DEPUY ORTHOPAEDICS INC US·Product code JDI·June 28, 2022
ENTERPRISE VASCULAR RECONSTRUCTION DEVICE AND DELIVERY SYSTEM
FDA Adverse Event
Malfunction
·CODMAN AND SHURTLEFF, INC·Product code NJE·September 22, 2015
UNK HIP ACETABULAR CUP PINNACLE
FDA Adverse Event
Malfunction
·DEPUY ORTHOPAEDICS INC US·Product code JDI·June 29, 2022