14 results
·
48ms
·
Sources: EU EUDAMED, US FDA
Filters
FDA Adverse Event
×
REVISION FEMORAL SYSTEM
FDA Adverse Event
Injury
·LIMACORPORATE S.P.A.·Product code LZO·March 27, 2024
SYRINGE 0.5ML 29G 12.7MM 10BAG 500 EU
FDA Adverse Event
Malfunction
·EMBECTA MEDICAL I LLC - HOLDREGE, NE·Product code FMF·May 22, 2025
SYRINGE 0.5ML 29G 12.7MM 10BAG 500 EU
FDA Adverse Event
Malfunction
·EMBECTA MEDICAL I LLC - HOLDREGE, NE·Product code FMF·May 22, 2025
SYRINGE 0.5ML 29G 12.7MM 10BAG 500 EU
FDA Adverse Event
Malfunction
·EMBECTA MEDICAL I LLC - HOLDREGE, NE·Product code FMF·May 22, 2025
FINESSE
FDA Adverse Event
Malfunction
·AMEDA.COM·Product code HGX·March 23, 2020
HEART START XL
FDA Adverse Event
Malfunction
·PHILIPS MEDICAL SYSTEMS·Product code MKJ·April 26, 2013
OT ULTRALINK METER
FDA Adverse Event
Malfunction
·LIFESCAN INC.·Product code NBW·May 23, 2011
LIGACLIP ENDOSCOPIC ROTATING MULTIPLE CLIP APPLIER 20 LARGE TITANIUM LIGATING CL
FDA Adverse Event
Malfunction
·ETHICON ENDO-SURGERY, LLC.·Product code FZP·August 5, 2008
ACTIVA
FDA Adverse Event
Malfunction
·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code MHY·August 31, 2016
ARROW AC3 OPTIMUS IABP NA/EMEA
FDA Adverse Event
Malfunction
·ARROW INTERNATIONAL LLC·Product code DSP·May 19, 2026
REVISION MODULAR STEM Ø16MM
FDA Adverse Event
Injury
·LIMACORPORATE S.P.A.·Product code LZO·June 22, 2022
AC3 OPTIMUS IABP NA/EMEA
FDA Adverse Event
Malfunction
·ARROW INTERNATIONAL LLC·Product code DSP·February 8, 2023
ARROW AC3 OPTIMUS IABP NA/EMEA
FDA Adverse Event
Malfunction
·ARROW INTERNATIONAL LLC·Product code DSP·March 8, 2024
ARROW AC3 OPTIMUS IABP NA/EMEA
FDA Adverse Event
Malfunction
·ARROW INTERNATIONAL LLC·Product code DSP·May 19, 2026