19 results
·
21ms
·
Sources: EU EUDAMED, US FDA
Filters
Status: Malfunction
×
6000023-1999-00068
FDA Adverse Event
Malfunction
·November 12, 1999
6000023-1999-00075
FDA Adverse Event
Malfunction
·November 12, 1999
6000023-1999-00076
FDA Adverse Event
Malfunction
·November 12, 1999
6000023-1999-00072
FDA Adverse Event
Malfunction
·November 12, 1999
6000023-1999-00073
FDA Adverse Event
Malfunction
·November 12, 1999
6000023-1999-00081
FDA Adverse Event
Malfunction
·November 12, 1999
6000023-1999-00069
FDA Adverse Event
Malfunction
·November 12, 1999
6000023-1999-00077
FDA Adverse Event
Malfunction
·November 12, 1999
6000023-1999-00070
FDA Adverse Event
Malfunction
·November 12, 1999
6000023-1999-00067
FDA Adverse Event
Malfunction
·September 8, 1999
6000023-1999-00063
FDA Adverse Event
Malfunction
·September 8, 1999
6000023-1999-00062
FDA Adverse Event
Malfunction
·September 8, 1999
RESTORE ULTRA
FDA Adverse Event
Malfunction
·MEDTRONIC MED REL MEDTRONIC PUERTO RICO·Product code LGW·October 8, 2012
DEVICE 8252600 NIM-RESPONSE 2.0 PATIENT
FDA Adverse Event
Malfunction
·MEDTRONIC XOMED, INC.·Product code ETN·March 8, 2013
INRATIO
FDA Adverse Event
Malfunction
·ALERE SAN DIEGO, INC.·Product code GJS·February 17, 2011
OASIS
FDA Adverse Event
Malfunction
·ATRIUM MEDICAL CORPORATION·Product code KDQ·February 28, 2025
OASIS
FDA Adverse Event
Malfunction
·ATRIUM MEDICAL CORPORATION·Product code KDQ·March 2, 2025
OASIS
FDA Adverse Event
Malfunction
·ATRIUM MEDICAL CORPORATION·Product code KDQ·March 2, 2025
OASIS
FDA Adverse Event
Malfunction
·ATRIUM MEDICAL CORPORATION·Product code KDQ·March 2, 2025