7 results
·
28ms
·
Sources: EU EUDAMED, US FDA
Filters
FDA Adverse Event
×
COIL EMBL 8CM 3MM AZUR CX
FDA Adverse Event
Malfunction
·TERUMO MEDICAL CANADA, INC.·Product code KRD·June 30, 2023
COIL EMBL 2CM 2MM AZUR CX
FDA Adverse Event
Malfunction
·TERUMO MEDICAL CANADA, INC.·Product code KRD·June 30, 2023
COIL EMBL 4CM 2MM AZUR CX
FDA Adverse Event
Malfunction
·TERUMO MEDICAL CANADA, INC.·Product code KRD·June 30, 2023
SPECTRUM INFUSION PUMP
FDA Adverse Event
Malfunction
·BAXTER HEALTHCARE CORPORATION·Product code FRN·January 3, 2014
OT VERIO IQ METER
FDA Adverse Event
Malfunction
·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·October 10, 2012
PUMP MMT-522LNAS PRDGM INS SK EN ML
FDA Adverse Event
Injury
·MEDTRONIC MINIMED·Product code LZG·July 26, 2010
AZUR CX 18D-LONGER
FDA Adverse Event
Malfunction
·MICROVENTION INC.·Product code KRD·September 11, 2024