10 results
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23ms
·
Sources: EU EUDAMED, US FDA
Filters
FDA Adverse Event
×
INNOVA 4100
FDA Adverse Event
Malfunction
·GE MEDICAL SYSTEMS·Product code MQB·April 4, 2011
INNOVA 4100
FDA Adverse Event
Malfunction
·GE MEDICAL SYSTEMS·Product code MQB·May 6, 2011
UNIVERSAL MODULAR ELECTRIC / BATTERY DOUBLE
FDA Adverse Event
Malfunction
·ZIMMER SURGICAL S.A.·Product code ERL·February 27, 2013
TOTAL CARE
FDA Adverse Event
Malfunction
·HILL-ROM, INC.·Product code FNL·February 15, 2011
COLLEAGUE CX VOLUMETRIC INFUSION PUMP
FDA Adverse Event
Malfunction
·BAXTER HEALTHCARE PTE LTD·Product code FRN·April 4, 2008
VUELOCK SCREW, UNKNOWN SIZE
FDA Adverse Event
Injury
·ZIMMER BIOMET SPINE INC.·Product code KWQ·April 16, 2020
VEULOCK SCREW, UNKNOWN SIZE
FDA Adverse Event
Injury
·ZIMMER BIOMET SPINE INC.·Product code KWQ·April 16, 2020
VEULOCK SCREW, UNKNOWN SIZE
FDA Adverse Event
Injury
·ZIMMER BIOMET SPINE INC.·Product code KWQ·April 16, 2020
VEULOCK SCREW, UNKNOWN SIZE
FDA Adverse Event
Injury
·ZIMMER BIOMET SPINE INC.·Product code KWQ·April 16, 2020
MINIMA STENT SYSTEM
FDA Adverse Event
Injury
·RENATA MEDICAL INC.·Product code QWC·December 19, 2023