15 results
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39ms
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Sources: EU EUDAMED, US FDA
Filters
FDA Adverse Event
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NO DEVICE
FDA Adverse Event
Injury
·ALLERGAN (COSTA RICA)·Product code FTR·February 4, 2025
SMR REVERSE HUMERAL BODY
FDA Adverse Event
Injury
·LIMACORPORATE S.P.A.·Product code KWS·October 21, 2022
PHYSICA FIXED TIBIAL PLATE #3
FDA Adverse Event
Injury
·LIMACORPORATE S.P.A.·Product code HRY·February 13, 2023
SAPPHIRE M.T INFUSION PUMP
FDA Adverse Event
Malfunction
·Q CORE MEDICAL LTD.·Product code FRN·November 16, 2015
6F ANGIO-SEAL VASCULAR CLOSURE DEVICE VIP
FDA Adverse Event
Injury
·ST. JUDE MEDICAL, PUERTO RICO, B.V.·Product code MGB·May 14, 2007
LIGACLIP** ENDOSCOPIC CLIP APPLIER
FDA Adverse Event
Malfunction
·ETHICON ENDO-SURGERY, LLC.·Product code FZP·March 12, 2013
UNKNOWN PREFILL
FDA Adverse Event
Malfunction
·COVIDIEN·Product code NZW·February 17, 2011
SMR CEMENTLESS FINNED STEM
FDA Adverse Event
Injury
·LIMACORPORATE S.P.A.·Product code HSD·December 21, 2020
POWERLED TM
FDA Adverse Event
Malfunction
·MAQUET SAS·Product code FSY·February 5, 2026
NEU_INTERSTIM_INS
FDA Adverse Event
Injury
·MEDTRONIC NEUROMODULATION·Product code EZW·July 12, 2012
SMR REVERSE FINNED HUMERAL BODY
FDA Adverse Event
Injury
·LIMACORPORATE S.P.A.·Product code KWS·February 4, 2022
OASIS
FDA Adverse Event
Malfunction
·ATRIUM MEDICAL CORPORATION·Product code KDQ·March 2, 2025
OASIS
FDA Adverse Event
Malfunction
·ATRIUM MEDICAL CORPORATION·Product code KDQ·March 2, 2025
OASIS
FDA Adverse Event
Malfunction
·ATRIUM MEDICAL CORPORATION·Product code KDQ·March 2, 2025
OASIS
FDA Adverse Event
Malfunction
·ATRIUM MEDICAL CORPORATION·Product code KDQ·March 2, 2025