10,000 results · 145ms · Sources: EU EUDAMED, US FDA

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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