1,270 results
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63ms
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Sources: EU EUDAMED, US FDA
Filters
Country: United States
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MOSS GASTROSTOMY TUBE (5-17719)
FDA Adverse Event
Death
·MOSS TUBES, INC.·Product code KNT·November 4, 2015
MOSS GASTROSTOMY TUBE
FDA Adverse Event
Malfunction
·MOSS TUBES, INC.·Product code KNT·August 27, 2020
MOSS MIAMI SCREW
FDA Adverse Event
Injury
·DEPUY SYNTHES SPINE·Product code KWP·June 9, 2014
MOSS MIAMI SCREW
FDA Adverse Event
Injury
·DEPUY SYNTHES SPINE·Product code KWP·June 9, 2014
MOSS MIAMI SCREW
FDA Adverse Event
Injury
·DEPUY SYNTHES SPINE·Product code KWP·June 9, 2014
MOSS MIAMI SPINAL SYSTEM
FDA Adverse Event
Other
·DEPUY ACROMED, INC.·Product code KWQ·May 15, 2002
DERMABOND PRINEO 22CM MSH 3.8ML ADHESIVE
FDA Adverse Event
Injury
·ETHICON INC.·Product code OMD·February 8, 2022
UNKNOWN SCREW/ROD CONSTRUCT ACCESSORIES
FDA Adverse Event
Injury
·MEDOS INTERNATIONAL SÃ RL CH·Product code MNH·December 23, 2019
UNKNOWN SCREWS
FDA Adverse Event
Injury
·MEDOS INTERNATIONAL SÃ RL CH·Product code HWC·October 25, 2019
UNKNOWN SCREWS
FDA Adverse Event
Injury
·MEDOS INTERNATIONAL SÃ RL CH·Product code HWC·October 25, 2019
UNKNOWN RODS
FDA Adverse Event
Injury
·MEDOS INTERNATIONAL SÃ RL CH·Product code HSB·October 25, 2019
MOSS MIAMI SPINE SYSTEM HEXLOBE DRIVER 5.5 X25
FDA Adverse Event
Malfunction
·DEPUY SPINE INC·Product code HWR·October 24, 2023
UNK_THERMOCOOL SF NAV
FDA Adverse Event
Injury
·BIOSENSE WEBSTER INC·Product code LPB·November 26, 2025
THORATEC® HEARTMATE 3® LVAS IMPLANT KIT
FDA Adverse Event
Death
·THORATEC CORPORATION·Product code DSQ·February 7, 2025
SURGIPRO
FDA Adverse Event
Injury
·COVIDIEN LP LLC NORTH HAVEN·Product code FTL·December 7, 2021
UNKNOWN PALMAZ STENT
FDA Adverse Event
Death
·CORDIS CASHEL·Product code FGE·October 29, 2018
UNKNOWN SCREW/ROD CONSTRUCT ACCESSORIES
FDA Adverse Event
Injury
·MEDOS INTERNATIONAL SÃ RL CH·Product code MNH·December 10, 2019
MOSS MIAMI SPINE SYSTEM HEXLOBE DRIVER 5.5 X25
FDA Adverse Event
Malfunction
·DEPUY SPINE INC·Product code HWR·October 24, 2023
UNKNOWN PALMAZ STENT
FDA Adverse Event
Injury
·CORDIS CASHEL·Product code FGE·November 5, 2018
UNKNOWN PALMAZ STENT
FDA Adverse Event
Injury
·CORDIS CASHEL·Product code FGE·November 5, 2018