8 results
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23ms
·
Sources: EU EUDAMED, US FDA
Filters
FDA Adverse Event
×
FRX DEFIBRILLATOR, ITALIAN, EXCHANGE
FDA Adverse Event
Malfunction
·PHILIPS NORTH AMERICA LLC·Product code MKJ·March 15, 2022
FRX (W B) DEFIB, THAI, EXCHG
FDA Adverse Event
Malfunction
·PHILIPS NORTH AMERICA LLC·Product code MKJ·March 15, 2022
HEARTSTART FRX DEFIBRILLATOR
FDA Adverse Event
Malfunction
·PHILIPS NORTH AMERICA LLC·Product code MKJ·May 26, 2022
NUCLEUS 22 CHANNEL COCHLEAR IMPLANT SYSTEM
FDA Adverse Event
Malfunction
·COCHLEAR LTD.·Product code MCM·August 23, 2016
EON MINI
FDA Adverse Event
Injury
·ST. JUDE MEDICAL - NEUROMODULATION·Product code GZB·October 15, 2014
ONETOUCHPING GLUCOSEMGMTSYSTEM
FDA Adverse Event
ANIMAS CORPORATION·Product code LZG·July 27, 2011
ADVANTAGE SERIES 26 OBS 10/04
FDA Adverse Event
Malfunction
·STRYKER MEDICAL-KALAMAZOO·Product code FPO·June 20, 2013
ENDOCARE CRYOCARE URETHRAL WARMING SYSTEM
FDA Adverse Event
Injury
·ENDOCARE INC.·Product code GEH·October 22, 2018