11 results
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39ms
·
Sources: EU EUDAMED, US FDA
Filters
FDA Adverse Event
×
INFUSOR
FDA Adverse Event
Malfunction
·BAXTER HEALTHCARE CORPORATION·Product code MEB·August 23, 2021
OT VERIO IQ METER
FDA Adverse Event
Malfunction
·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·April 8, 2013
ENDOTAK RELIANCE
FDA Adverse Event
Malfunction
·CPI - DEL CARIBE·Product code NVY·April 6, 2011
CONTAK RENEWAL 3
FDA Adverse Event
Malfunction
·CARDIAC PACEMAKERS, INC·Product code NIK·May 8, 2008
CE INFUSOR LV 2, 12 PACK
FDA Adverse Event
Malfunction
·BAXTER HEALTHCARE - IRVINE·Product code MEB·July 14, 2010
CE INFUSOR SV 2, 12 PACK
FDA Adverse Event
Malfunction
·BAXTER HEALTHCARE - IRVINE·Product code FRN·March 10, 2010
INTERSTIM
FDA Adverse Event
Malfunction
·AVAILMED S.A.DE C.V.9·Product code EZW·July 17, 2020
INTERSTIM
FDA Adverse Event
Malfunction
·AVAILMED S.A.DE C.V.9·Product code EZW·June 18, 2020
VERIFY ENHANCED
FDA Adverse Event
Malfunction
·MEDTRONIC NEUROMODULATION·Product code EZW·December 6, 2024
SURESCAN
FDA Adverse Event
Malfunction
·MPRI·Product code EZW·February 11, 2021
SURESCAN
FDA Adverse Event
Malfunction
·MPRI·Product code EZW·February 25, 2021