594 results
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29ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: 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