8 results
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18ms
·
Sources: EU EUDAMED, US FDA
Filters
Status: Malfunction
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BD SYRINGE 5ML LL SP125
FDA Adverse Event
Malfunction
·BECTON DICKINSON MEDICAL SYSTEMS·Product code FMF·October 9, 2024
ASSURE PLATINUM BLOOD GLUCOSE SYSTEM
FDA Adverse Event
Malfunction
·ARKRAY, INC.·Product code NBW·June 5, 2014
OT VERIO IQ METER
FDA Adverse Event
Malfunction
·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·September 26, 2015
ASSURE PLATINUM BLOOD GLUCOSE SYSTEM
FDA Adverse Event
Malfunction
·ARKRAY, INC.·Product code NBW·June 5, 2014
VERTEX RECONSTRUCTION SYSTEM
FDA Adverse Event
Malfunction
·WARSAW ORTHOPEDICS·Product code KWP·October 18, 2018
LIFEPAK(R) 12 DEFIBRILLATOR/MONITOR SERIES
FDA Adverse Event
Malfunction
·PHYSIO-CONTROL, INC·Product code MKJ·May 21, 2013
INTERMATE
FDA Adverse Event
Malfunction
·BAXTER HEALTHCARE - IRVINE·Product code FRN·September 26, 2014
VERTEX® RECONSTRUCTION SYSTEM
FDA Adverse Event
Malfunction
·WARSAW ORTHOPEDICS·Product code KWP·July 15, 2024