C.R. Bard Recalls
117 recalls on record · November 12, 2014 to May 27, 2026 · Medical Devices
Recalls by year
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Count of recall notices naming this brand, by the year the recall was announced. A quiet year is not proof of a safe year.
January 31, 2024Medical DevicesFDA
C.R. Bard Inc recalls Bard¿ Nasogastric Sump Tube with ENFit, 18Fr., 48in Long, REF EN0042180
Hazard: BD (C.R. Bard) has received user complaints reporting that during use of BD Bard NG Sump Tubes with ENFit Connectors, inadequate or reduced suction, decompression, and drainage occurred.
January 31, 2024Medical DevicesFDA
C.R. Bard Inc recalls Bard¿ Nasogastric Sump Tube with ENFit, 16Fr., 48in Long, REF EN0042160
Hazard: BD (C.R. Bard) has received user complaints reporting that during use of BD Bard NG Sump Tubes with ENFit Connectors, inadequate or reduced suction, decompression, and drainage occurred.
January 31, 2024Medical DevicesFDA
C.R. Bard Inc recalls Bard¿ Nasogastric Sump Tube with ENFit, 14Fr., 48in Long, REF EN0042140
Hazard: BD (C.R. Bard) has received user complaints reporting that during use of BD Bard NG Sump Tubes with ENFit Connectors, inadequate or reduced suction, decompression, and drainage occurred.
January 31, 2024Medical DevicesFDA
C.R. Bard Inc recalls Bard¿ Nasogastric Sump Tube with ENFit, 12Fr., 48in Long, REF EN0042120
Hazard: BD (C.R. Bard) has received user complaints reporting that during use of BD Bard NG Sump Tubes with ENFit Connectors, inadequate or reduced suction, decompression, and drainage occurred.
January 31, 2024Medical DevicesFDA
C.R. Bard Inc recalls Bard Nasogastric Sump Tube with ENFit, 10Fr., 36in Long, REF EN0042100
Hazard: BD (C.R. Bard) has received user complaints reporting that during use of BD Bard NG Sump Tubes with ENFit Connectors, inadequate or reduced suction, decompression, and drainage occurred.
December 20, 2023Medical DevicesFDA
C.R. Bard Inc recalls Sensica Urine Output System, Catalog Number SCCS1002
Hazard: BD (C.R. Bard) has received user complaints reporting that when the device was connected to WiFi/Internet, the time displayed on the Sensica device changed during a patient monitoring session which resulted in 1) incorrect time displayed on the monitoring screen, 2) incorrect hour block timestamps on the monitoring screen, 3) incorrect hour timestamps on data screens, and 4) incorrect catheter use time.
June 14, 2023Medical DevicesFDA
C.R. Bard Inc recalls HydroSil Go Intermittent Urinary Catheters, Catalog Numbers: a) REF 71808, b) REF 71810, c) REF 71812, d) REF 71814, e)
Hazard: Some catheters had a manufacturing defect where the clear resealing label separating from the product foil pouch, resulting in a possible opening into the product packaging that could impact product sterility.
June 14, 2023Medical DevicesFDA
C.R. Bard Inc recalls Magic3 Go Intermittent Urinary Catheters, pediatric Catalog Numbers: a) REF 52810G
Hazard: Some catheters had a manufacturing defect where the clear resealing label separating from the product foil pouch, resulting in a possible opening into the product packaging that could impact product sterility.
June 14, 2023Medical DevicesFDA
C.R. Bard Inc recalls Magic3 Go Intermittent Urinary Catheters, male Catalog Numbers: a) REF 50810G, b) REF 50812G, c) REF 50814G, d) REF 5081
Hazard: Some catheters had a manufacturing defect where the clear resealing label separating from the product foil pouch, resulting in a possible opening into the product packaging that could impact product sterility.
June 14, 2023Medical DevicesFDA
C.R. Bard Inc recalls Magic3 Go Intermittent Urinary Catheters, Female Catalog Numbers: a) REF 51808, b) REF 51810, c) REF 51812, d) REF 51814
Hazard: Some catheters had a manufacturing defect where the clear resealing label separating from the product foil pouch, resulting in a possible opening into the product packaging that could impact product sterility.
July 6, 2022Medical DevicesFDA
C.R. Bard Inc recalls Sensica Urine Output System
Hazard: Complaints relating to urine output measurement accuracy.
March 2, 2022Medical DevicesFDA
C.R. Bard Inc recalls BARD SURESTEP INTERMITTENT CATHETER TRAY, 14Fr, REF INTS16C
Hazard: There is a potential to leak from the catheter where it connects to the drain bag
March 2, 2022Medical DevicesFDA
C.R. Bard Inc recalls BARD SURESTEP INTERMITTENT CATHETER TRAY, 14Fr, REF INTS14C
Hazard: There is a potential to leak from the catheter where it connects to the drain bag
September 29, 2021Medical DevicesFDA
C.R. Bard Inc recalls Catalog A942216, SureStep" Foley Tray, Bard LubricathTM, Urine Meter, StatLock" Stabilization Device
Hazard: There is potential for packaging defects that may impact the sterile barrier.
September 29, 2021Medical DevicesFDA
C.R. Bard Inc recalls Catalog A303416A, SureStep" Foley Tray, Lubri-Sil" I.C., Temperature Sensing Complete Care", Drainage Bag, StatLock" Sta
Hazard: There is potential for packaging defects that may impact the sterile barrier.
September 29, 2021Medical DevicesFDA
C.R. Bard Inc recalls Catalog A902416, SureStep" Foley Tray, Silicone, Urine Meter, StatLock" Stabilization Device
Hazard: There is potential for packaging defects that may impact the sterile barrier.
September 29, 2021Medical DevicesFDA
C.R. Bard Inc recalls Catalog A319516AM, SureStep" Foley Tray, Lubri-Sil" I.C., Temperature Sensing Complete Care", Drainage Bag, StatLock" St
Hazard: There is potential for packaging defects that may impact the sterile barrier.
September 29, 2021Medical DevicesFDA
C.R. Bard Inc recalls Catalog A943216, SureStep" Foley Tray, Lubricath", Urine Meter, StatLock" Stabilization Device
Hazard: There is potential for packaging defects that may impact the sterile barrier.
September 29, 2021Medical DevicesFDA
C.R. Bard Inc recalls Catalog A902916, SureStep" Foley Tray, Lubricath", Urine Meter, StatLock" Stabilization Device
Hazard: There is potential for packaging defects that may impact the sterile barrier.
September 29, 2021Medical DevicesFDA
C.R. Bard Inc recalls Catalog A902616, SureStep" Foley Tray, Bardex" I.C., Lubricath", Urine Meter
Hazard: There is potential for packaging defects that may impact the sterile barrier.
September 29, 2021Medical DevicesFDA
C.R. Bard Inc recalls Catalog A899916, SureStep" Foley Tray, Lubricath", Drainage Bag, StatLock" Stabilization Device
Hazard: There is potential for packaging defects that may impact the sterile barrier.
September 29, 2021Medical DevicesFDA
C.R. Bard Inc recalls Catalog A897514, SureStep" Foley Tray, Silicone, Drainage Bag, StatLock" Stabilization Device
Hazard: There is potential for packaging defects that may impact the sterile barrier.
September 29, 2021Medical DevicesFDA
C.R. Bard Inc recalls Catalog A800365, SureStep" Foley Tray, Bard LubricathTM Foley Catheter Tray
Hazard: There is potential for packaging defects that may impact the sterile barrier.
September 29, 2021Medical DevicesFDA
C.R. Bard Inc recalls Catalog A800361, SureStep" Foley Tray, Bard LubricathTM Foley Catheter Tray
Hazard: There is potential for packaging defects that may impact the sterile barrier.
September 29, 2021Medical DevicesFDA
C.R. Bard Inc recalls Catalog A800360, SureStep" Foley Tray, Bard LubricathTM Foley Catheter Tray
Hazard: There is potential for packaging defects that may impact the sterile barrier.
September 29, 2021Medical DevicesFDA
C.R. Bard Inc recalls Catalog A800061, SureStep" Foley Tray, Bard LubricathTM Foley Catheter Tray
Hazard: There is potential for packaging defects that may impact the sterile barrier.
September 29, 2021Medical DevicesFDA
C.R. Bard Inc recalls Catalog A399400A, SureStep" Foley Tray, Add-a-Foley, Complete Care", Drainage Bag, StatLock" Stabilization Device
Hazard: There is potential for packaging defects that may impact the sterile barrier.
September 29, 2021Medical DevicesFDA
C.R. Bard Inc recalls Catalog A319416AM, SureStep" Foley Tray, Bardex" I.C., Complete Care", Urine Meter, Temperature Sensing, StatLock" Stabi
Hazard: There is potential for packaging defects that may impact the sterile barrier.
September 29, 2021Medical DevicesFDA
C.R. Bard Inc recalls Catalog A303318A, SureStep" Foley Tray, Bardex" I.C., Complete Care", Urine Meter, StatLock" Stabilization Device
Hazard: There is potential for packaging defects that may impact the sterile barrier.
September 29, 2021Medical DevicesFDA
C.R. Bard Inc recalls Catalog A303316A, SureStep" Foley Tray, Bardex" I.C., Complete Care", Urine Meter, StatLock" Stabilization Device
Hazard: There is potential for packaging defects that may impact the sterile barrier.