191 results
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65ms
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Sources: EU EUDAMED, US FDA
BARD MEDICAL DIVISION
FDA Adverse Event
Injury
·C.R. BARD, INC.·Product code KOD·March 30, 2000
BARD MEDICAL DIVISION
FDA Adverse Event
Injury
·C.R. BARD, INC.·Product code KOD·March 30, 2000
MAGIC HYDROPHILIC-COATED FEMALE INTERMITTENT CATHETER 14 FR
FDA Adverse Event
Injury
·BARD MEDICAL·Product code KOD·July 19, 2015
ROCHESTER MEC WIDEBAND M 100BX
FDA Adverse Event
Malfunction
·DAVOL SURGICAL INNOVATIONS -9616067·Product code NNX·June 22, 2017
BARDEX 5CC LUBRICATH 2-WAY LATEX FOLEY CATHETER
FDA Adverse Event
Death
·C.R. BARD, INC. (MONCKS) -1030583·Product code EZC·October 5, 2015
DIMENSION ARTICULATING STONE BASKET/GRASPER
FDA Adverse Event
Malfunction
·OMNITECH SYSTEMS, INC.·Product code FFL·September 26, 2014
INTERMITTENT HYDROPHILIC URINARY COUDE CATHETER
FDA Adverse Event
Malfunction
·ROCHESTER MEDICAL CORP. 2130787·Product code KOD·February 17, 2015
BARD URINARY 2 LITER DRAINAGE BAG WITH ANTI-REFLUX CHAMBER
FDA Adverse Event
Malfunction
·PRODUCTOS PARA EL CUIDADO DE LA SALUD·Product code KNX·December 16, 2014
BARD URINARY 2 LITE DRAINAGE BAG WITH ANTI-REFLUX CHAMBER
FDA Adverse Event
Malfunction
·PRODUCTOS PARA EL CUIDADO DE LA SALUD·Product code KNX·December 16, 2014
BARDEX 5CC LUBRICATH 2-WAY LATEX FOLEY CATHETER
FDA Adverse Event
Injury
·C.R. BARD, INC. (MONCKS) -1030583·Product code EZC·October 5, 2015
LUBRI-SIL I/C FOLEY TRAY
FDA Adverse Event
Malfunction
·PRODUCTOS PARA EL CUIDADO DE LA SALUD·Product code MJC·October 29, 2012
BARD DIAGNOSTIC WOVEN QUAD CATHETER
FDA Adverse Event
Injury
·BARD MEDICAL DIVISION·Product code DRF·August 12, 2023
BARDIA RED RUBBER URETHRAL COUDE CATHETER, 16 FR.
FDA Adverse Event
Malfunction
·C.R. BARD, INC. (MONCKS) -1030583·Product code EZC·April 12, 2017
FLUORO-4 COIL STENT
FDA Adverse Event
Malfunction
·PRODUCTOS PARA EL CUIDADO DE LA SALUD·Product code FAD·October 29, 2012
BARD¿ BrachySource¿ Iodine125 radioactive seeds consist of a welded titanium capsule containing the I125 absorbed onto a nickel / copper-coated, gold-cored aluminum wire (reference Figure 1 below). The I125 has a half-life of 59.6 days and decays by electron capture with the emission of characteristic photons and Auger electrons. The principal photon emissions are 27.4 and 31 keV x-rays and 35.5 keV gamma. The titanium wall of the BrachySource¿ Seed Implants absorbs the electrons.
FDA Enforcement
Class II
·Terminated·Bard Brachytherapy, Inc.·May 16, 2018
THERMOCOOL® SF UNI-DIRECTIONAL CATHETER
FDA Adverse Event
Injury
·BIOSENSE WEBSTER, INC (IRWINDALE)·Product code LPB·August 4, 2014
THERMOCOOL® SMARTTOUCH® BI-DIRECTIONAL NAVIGATION CATHETER
FDA Adverse Event
Injury
·BIOSENSE WEBSTER, INC (IRWINDALE)·Product code LPB·April 4, 2014
BARD BrachySource Iodine125 radioactive seeds consist of a welded titanium capsule containing the I125 absorbed onto a nickel / copper-coated, gold-cored aluminum wire (reference Figure 1 below). The I125 has a half-life of 59.6 days and decays by electron capture with the emission of characteristic photons and Auger electrons. The principal photon emissions are 27.4 and 31 keV x-rays and 35.5 keV gamma. The titanium wall of the BrachySource Seed Implants absorbs the electrons.
FDA Recall
Terminated
·Bard Brachytherapy, Inc.·Product code KXK·April 10, 2018
BARD POWERPICC
FDA Adverse Event
Malfunction
·BARD MEDICAL DIVISION, BARD MEDICAL·Product code LJS·December 22, 2009
BARDEX IC COMPLETE CARE FOLEY TRAY
FDA Adverse Event
Malfunction
·PRODUCTOS PARA EL CUIDADO DE LA SALUD·Product code MJC·August 10, 2012