20 results
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31ms
·
Sources: EU EUDAMED, US FDA
Filters
FDA Adverse Event
×
VIDAS RUB IGG II 60 TESTS
FDA Adverse Event
Malfunction
·BIOMERIEUX SA·Product code LFX·April 3, 2020
ESSURE
FDA Adverse Event
Injury
·CONCEPTUS·Product code HHS·February 12, 2014
ESSURE
FDA Adverse Event
Injury
·CONCEPTUS·Product code HHS·February 12, 2014
MEDSTONE LITHOTRIPTOR
FDA Adverse Event
Malfunction
·HEALTHTRONICS, INC.·Product code LNS·June 12, 2017
OT VERIO METER
FDA Adverse Event
Malfunction
·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·March 19, 2013
BHR
FDA Adverse Event
Injury
·SMITH & NEPHEW ORTHOPAEDICS, LTD.·Product code NXT·March 8, 2011
LIFEPAK 500 AUTOMATED EXTERNAL DEFIBRILLATOR
FDA Adverse Event
Malfunction
·PHYSIO-CONTROL, INC.·Product code MKJ·March 10, 2008
MICRUS MICROCOIL SYSTEM
FDA Adverse Event
Injury
·MICRUS ENDOVASCULAR CORPORATION·Product code MJN·February 10, 2012
BD SYRINGE 50ML LL
FDA Adverse Event
Malfunction
·BECTON DICKINSON, S.A.·Product code FMF·May 14, 2021
450 SAL EJECTOR 3283
FDA Adverse Event
Malfunction
·COVIDIEN·Product code DYN·June 23, 2016
UNKNOWN KNEE PATELLA
FDA Adverse Event
Injury
·DEPUY ORTHOPAEDICS INC US·Product code JWH·December 3, 2019
UNKNOWN KNEE FEMORAL
FDA Adverse Event
Injury
·DEPUY ORTHOPAEDICS INC US·Product code JWH·December 3, 2019
BD PLASTIPAK 50ML CONCENTRIC LUER LOCK SYRINGE
FDA Adverse Event
Malfunction
·BECTON DICKINSON, S.A.·Product code FMF·April 15, 2021
METAL METAL BALL HEAD 28L CONE
FDA Adverse Event
Injury
·SMITH & NEPHEW ORTHOPAEDICS AG·Product code LPH·April 15, 2022
ULTRA SHORT STRUT TL-HEX - 45MM-101MM
FDA Adverse Event
Injury
·ORTHOFIX SRL·Product code KTT·April 4, 2017
ULTRA SHORT STRUT TL-HEX - 45MM-101MM
FDA Adverse Event
Injury
·ORTHOFIX SRL·Product code KTT·April 27, 2016
VIDAS RUB IGG II 60 TESTS - 30221
FDA Adverse Event
Malfunction
·BIOMÉRIEUX, SA·Product code LFX·March 19, 2020
ULTRA SHORT STRUT TL-HEX - 45MM-101MM
FDA Adverse Event
Malfunction
·ORTHOFIX SRL·Product code KTT·September 21, 2016
MODULAR 5/8 RING, 160MM, TL-HEX
FDA Adverse Event
Injury
·ORTHOFIX SRL·Product code KTT·April 27, 2016
BICON-PLUS PE INSERT ANTIL 3/28 NON-CEM
FDA Adverse Event
Injury
·SMITH & NEPHEW ORTHOPAEDICS AG·Product code JDG·March 20, 2022