25 results · 26ms · Sources: EU EUDAMED, US FDA

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STEELEX STE SET 6 (8) 4X45CM HRS48

FDA Adverse Event
Malfunction ·B. BRAUN SURGICAL S.A.·Product code GAQ·February 7, 2014

REMSTAR AUTO

FDA Adverse Event
Malfunction ·RESPIRONICS, INC.·Product code BZD·August 20, 2021

REMSTAR PRO

FDA Adverse Event
Malfunction ·RESPIRONICS, INC.·Product code BZD·August 20, 2021

REMSTAR AUTO A-FLEX W/HUMID

FDA Adverse Event
Malfunction ·RESPIRONICS, INC·Product code BZD·August 10, 2021

REMSTAR AUTO A-FLEX, SYS ONE, 60 SRS, FR

FDA Adverse Event
Injury ·RESPIRONICS, INC·Product code BZD·August 5, 2021

REMSTAR AUTO A-FLEX, SYS ONE, 60 SRS,GER

FDA Adverse Event
Injury ·RESPIRONICS INC·Product code BZD·August 30, 2021

REMSTAR PRO C-FLEX+

FDA Adverse Event
Malfunction ·RESPIRONICS INC·Product code BZD·February 8, 2022

9800

FDA Adverse Event
Malfunction ·GE OEC MEDICAL SYSTEMS (SCL)·Product code JAA·May 9, 2013

MECHANICAL WALKER, ROLLATOR

FDA Adverse Event
CONSMA·Product code ITJ·September 24, 2014

ASR ACETABULAR IMPLANT 50

FDA Adverse Event
Injury ·DEPUY INTERNATIONAL, LTD.·Product code KWA·May 18, 2011

CHPV RT ANG RESERVOIR UNITIZED

FDA Adverse Event
Injury ·INTEGRA LIFESCIENCES MANSFIELD·Product code JXG·January 17, 2024

REMSTAR PRO C-FLEX+

FDA Adverse Event
Malfunction ·RESPIRONICS INC·Product code BZD·February 8, 2022

MD HYBRID GLENOID BASE 4MM

FDA Adverse Event
Injury ·ZIMMER BIOMET, INC.·Product code HSD·June 27, 2023

REMSTAR AUTO A-FLEX

FDA Adverse Event
Malfunction ·RESPIRONICS, INC.·Product code BZD·January 14, 2022

REMSTAR AUTO A-FLEX W/SD CARD, GER

FDA Adverse Event
Malfunction ·RESPIRONICS INC·Product code BZD·August 5, 2021

REMSTAR AUTO W/HT HUM,SYS ONE,60 SRS,CAN

FDA Adverse Event
Injury ·RESPIRONICS, INC.·Product code BZD·August 3, 2021

REMSTAR AUTO A-FLEX, SYS ONE, 60 SRS,DOM

FDA Adverse Event
Malfunction ·RESPIRONICS, INC·Product code BZD·July 30, 2021

REMSTAR AUTOA-FLEX W/ HUM, SYSONE 60SRS, AUS

FDA Adverse Event
Injury ·RESPORINOC INC·Product code BZD·August 11, 2021

REMSTAR AUTO A-FLEX

FDA Adverse Event
Malfunction ·RESPIRONICS, INC.·Product code BZD·July 18, 2022

HYBRID GLENOID POROUS TITANIUM GLENOID POST

FDA Adverse Event
Injury ·BIOMET ORTHOPEDICS·Product code KWS·January 6, 2017