594 results · 29ms · Sources: EU EUDAMED, US FDA

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PARADIGM REAL-TIME REVEL INSULIN INFUSION PUMP

FDA Adverse Event
Malfunction ·MEDTRONIC MINIMED·Product code OYC·February 28, 2017

640G INSULIN PUMP

FDA Adverse Event
Malfunction ·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code OYC·January 4, 2016

PARADIGM REAL-TIME INSULIN INFUSION PUMP MMT-754LCMS

FDA Adverse Event
Malfunction ·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code OYC·August 18, 2025

HURST ESOPHAGEAL BOUGIE 30 FR

FDA Adverse Event
Malfunction ·TELEFLEX MEDICAL·Product code KCD·January 11, 2010

MALONEY TUNGSTEN FILLED BOUGIE 34F

FDA Adverse Event
Malfunction ·TELEFLEX·Product code KCD·May 5, 2014

RUSCH HURST ESOPHAGEAL BOUGIE 3

FDA Adverse Event
Malfunction ·TELEFLEX MEDICAL·Product code KCD·January 9, 2014

MALONEY TAPERED MERCURY-FILLED ESOPHAGEAL BOUGIES

FDA Adverse Event
PILLING COMPANY·Product code KCD·January 23, 1995

KARL STORZ

FDA Adverse Event
Injury ·KARL STORZ GMBH & CO.·Product code KCD·October 13, 2000

9610617-2000-00022

FDA Adverse Event
Death ·Product code KCD·October 13, 2000

MALONEY ESPOHAGEAL BOUGIE

FDA Adverse Event
Malfunction ·RUSCH, INC.·Product code KCD·January 5, 2000

RUSCH MALONEY ESOPHAGEAL BOUGIE

FDA Adverse Event
Malfunction ·TELEFLEX MEDICAL·Product code KCD·November 1, 2011

RUSCH HURST ESOPHAGEAL BOUGIE

FDA Adverse Event
Malfunction ·TELEFLEX MEDICAL·Product code KCD·June 6, 2011

RUSCH MALONEY ESOPHAGEAL BOUGIE 58F

FDA Adverse Event
Malfunction ·TELEFLEX MEDICAL·Product code KCD·July 18, 2012

RUSCH MALONEY ESOPHAGEAL BOUGIE

FDA Adverse Event
Malfunction ·TELEFLEX MEDICAL·Product code KCD·September 18, 2008

PILLING

FDA Adverse Event
Injury ·TELEFLEX MEDICAL·Product code KCD·January 24, 2019

MALONEY BOUGIE

FDA Adverse Event
Injury ·PILLING·Product code KCD·July 9, 1992

PILLING WECK

FDA Adverse Event
Injury ·PILLING WECK·Product code KCD·September 14, 1999

ENDOLUMINA II TRANSILLUMINATED BOUGIE

FDA Adverse Event
Malfunction ·BIOENTERICS CORPORATION·Product code KCD·February 3, 1998

MALONEY 60FR ESOPHAGEAL BOUGIE

FDA Adverse Event
Injury ·RUSCH, INC.·Product code KCD·December 8, 1997

RUSCH

FDA Adverse Event
Malfunction ·RUSCH, INC.·Product code KCD·August 16, 2001