191 results · 65ms · Sources: EU EUDAMED, US FDA

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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