8 results
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21ms
·
Sources: EU EUDAMED, US FDA
Filters
FDA Adverse Event
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BD PLASTIC NON-STERILE 5ML LUER-LOK¿ TIP SYRINGE
FDA Adverse Event
Malfunction
·BECTON DICKINSON MEDICAL SYSTEMS·Product code FMF·September 20, 2017
ONYX
FDA Adverse Event
Malfunction
·EV3 NEUROVASCULAR·Product code MFE·November 4, 2009
IN TOUCH ZU
FDA Adverse Event
Malfunction
·STRYKER MEDICAL-KALAMAZOO·Product code FNL·March 13, 2013
UNKNOWN DEPUY DURALOC 28X52 10D LINER
FDA Adverse Event
Injury
·DEPUY ORTHOPAEDICS, INC.·Product code LPH·February 16, 2011
COVIDIEN/KENDALL
FDA Adverse Event
Malfunction
·COVIDIEN·Product code LZH·February 21, 2008
GMK SPHERE TOTAL KNEE SYSTEM
FDA Adverse Event
Injury
·MEDACTA INTERNATIONAL SA·Product code JWH·November 21, 2025
SYNCARDIA COMPANION EXTERNAL LI-BATTERY PACK
FDA Adverse Event
Malfunction
·SYNCARDIA SYSTEMS, INC.·Product code LOZ·December 11, 2014
SYNCARDIA COMPANION EXTERNAL LI-BATTERY PACK
FDA Adverse Event
Malfunction
·SYNCARDIA SYSTEMS, INC.·Product code LOZ·December 11, 2014