10,000 results
·
145ms
·
Sources: EU EUDAMED, US FDA
Filters
Status: Malfunction
×
MEDTRONIC
FDA Adverse Event
Malfunction
·REP. SUPPLIED INSTRUMENTATION·Product code MQP·June 8, 2005
MEDTRONIC
FDA Adverse Event
Malfunction
·REP - WILL LALLY·Product code LGW·August 6, 2009
VITAL CARE
FDA Adverse Event
Malfunction
·VITAL CARE REPS, INC.·Product code KKX·January 9, 2003
REP DREAMSTATION
FDA Adverse Event
Malfunction
·RESPIRONICS, INC.·Product code BZD·March 10, 2024
BICEPS TENODESIS REP
FDA Adverse Event
Malfunction
·MANSFIELD·Product code HWC·May 13, 2010
REP DREAMSTATION AUTO
FDA Adverse Event
Malfunction
·RESPIRONICS, INC.·Product code BZD·October 27, 2023
BICEPS TENODESIS REP
FDA Adverse Event
Malfunction
·SMITH & NEPHEW ENDOSCOPY·Product code MBI·November 18, 2011
REP DREAMSTATION ST30
FDA Adverse Event
Malfunction
·RESPIRONICS, INC.·Product code MNS·October 21, 2024
REP DREAMSTATION BIPAP
FDA Adverse Event
Malfunction
·RESPIRONICS, INC.·Product code MNS·May 22, 2025
REP DREAMSTATION AUTO
FDA Adverse Event
Malfunction
·RESPIRONICS, INC.·Product code BZD·March 18, 2025
REP DREAMSTATION AUTO
FDA Adverse Event
Malfunction
·RESPIRONICS, INC.·Product code BZD·February 4, 2025
REP DREAMSTATION AVAPS30
FDA Adverse Event
Malfunction
·RESPIRONICS, INC.·Product code MNS·January 3, 2026
REP DREAMSTATION AUTO
FDA Adverse Event
Malfunction
·RESPIRONICS, INC.·Product code BZD·February 23, 2025
REP DREAMSTATION AUTO
FDA Adverse Event
Malfunction
·RESPIRONICS, INC.·Product code BZD·February 4, 2025
REP DREAMSTATION AUTO
FDA Adverse Event
Malfunction
·RESPIRONICS, INC.·Product code BZD·February 22, 2025
REP DREAMSTATION AUTO
FDA Adverse Event
Malfunction
·RESPIRONICS, INC.·Product code BZD·February 4, 2025
BICEPS TENODESIS REP
FDA Adverse Event
Malfunction
·SMITH & NEPHEW ENDOSCOPY·Product code HRX·August 25, 2010
REP DREAMSTATION AUTO BIPAP
FDA Adverse Event
Malfunction
·RESPIRONICS,INC·Product code BZD·June 17, 2022
REP DREAMSTATION AUTO CPAP
FDA Adverse Event
Malfunction
·RESPIRONICS, INC.·Product code BZD·October 25, 2021
SERVICE REP, MDU,ULTRALIGHT
FDA Adverse Event
Malfunction
·SMITH & NEPHEW, INC.·Product code HAB·July 21, 2015