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Bard Peripheral Vascular Recalls
139 recalls on record · June 19, 2013 to February 25, 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.
September 4, 2019Medical DevicesFDA
Bard Peripheral Vascular Inc recalls EQUISTREAM LONG-TERM HEMODIALYSIS CATHETER, REF/Product code:5905240, 14.5 Fr. Alphacurve Catheter with Standard Kit, 24
Hazard: The action is being initiated due to complaints received concerning the molded tip of the tunneler breaking or is damaged during the placement procedure of the catheter.
September 4, 2019Medical DevicesFDA
Bard Peripheral Vascular Inc recalls EQUISTREAM LONG-TERM HEMODIALYSIS CATHETER, REF/Product Code:5905190, 14.5 Fr. Alphacurve Catheter with Standard Kit, 19
Hazard: The action is being initiated due to complaints received concerning the molded tip of the tunneler breaking or is damaged during the placement procedure of the catheter.
August 14, 2019Medical DevicesFDA
Bard Peripheral Vascular Inc recalls EnCor Breast Biopsy Probes, packaged individually in sterile pouches, 5 pouches/carton, single use, Rx, catalog/REF numb
Hazard: There has been an increase in complaints related to leaks, suction issues, and failure to obtain samples while using the product.
August 14, 2019Medical DevicesFDA
Bard Peripheral Vascular Inc recalls EnCor Breast Biopsy Probes, packaged individually in sterile pouches, 5 pouches/carton, single use, Rx, catalog/REF numb
Hazard: There has been an increase in complaints related to leaks, suction issues, and failure to obtain samples while using the product.
August 14, 2019Medical DevicesFDA
Bard Peripheral Vascular Inc recalls EnCor Breast Biopsy Probes, packaged individually in sterile pouches, 5 pouches/carton, single use, Rx, catalog/REF numb
Hazard: There has been an increase in complaints related to leaks, suction issues, and failure to obtain samples while using the product.
August 14, 2019Medical DevicesFDA
Bard Peripheral Vascular Inc recalls EnCor Breast Biopsy Probes, packaged individually in sterile pouches, 5 pouches/carton, single use, Rx, catalog/REF numb
Hazard: There has been an increase in complaints related to leaks, suction issues, and failure to obtain samples while using the product.
August 14, 2019Medical DevicesFDA
Bard Peripheral Vascular Inc recalls EnCor Breast Biopsy Probes, packaged individually in sterile pouches, 5 pouches/carton, single use, Rx, catalog/REF numb
Hazard: There has been an increase in complaints related to leaks, suction issues, and failure to obtain samples while using the product.
August 14, 2019Medical DevicesFDA
Bard Peripheral Vascular Inc recalls EnCor Breast Biopsy Probes, packaged individually in sterile pouches, 5 pouches/carton, single use, Rx, catalog/REF numb
Hazard: There has been an increase in complaints related to leaks, suction issues, and failure to obtain samples while using the product.
July 31, 2019Medical DevicesFDA
Bard Peripheral Vascular Inc recalls POWERPORT CLEARVUE isp, 6F CHRONOFLEX Catheter, Intermediate NAUTILUS DELTA Kit; POWERPORT CLEARVUE isp, 8F CHRONOFLE
Hazard: Certain NAUTILUS DELTA Port Kit product code / lot number combinations may be at risk of experiencing a lack of or a loss of the intravascular ECG signal during port placement procedures when used in combination with the NAUTILUS DELTA" TCS.
May 23, 2018Medical DevicesFDA
Bard Peripheral Vascular Inc recalls BARD PERIPHERAL VASCULAR SEEKER(R) Crossing Support Catheter, 0.014", 150 cm, REF SK15014. Intended to support a guid
Hazard: Device is at risk of having detectable levels of bacterial endotoxin present on the packaging hoop that the catheter is packaged in. The bacterial endotoxin levels for the catheters are within acceptable levels; however, if bacterial endotoxins are present on the packaging hoops it may have the potential for cross-contamination in a clinical setting.
May 23, 2018Medical DevicesFDA
Bard Peripheral Vascular Inc recalls BARD PERIPHERAL VASCULAR SEEKER(R) Crossing Support Catheter, 0.035", 150 cm, REF SK15035M. Intended to support a gui
Hazard: Device is at risk of having detectable levels of bacterial endotoxin present on the packaging hoop that the catheter is packaged in. The bacterial endotoxin levels for the catheters are within acceptable levels; however, if bacterial endotoxins are present on the packaging hoops it may have the potential for cross-contamination in a clinical setting.
May 16, 2018Medical DevicesFDA
Bard Peripheral Vascular Inc recalls POWERPORT ClearVUE Slim Implantable Port with Smooth Septum and Attachable 8F Polyurethane Open-Ended Single-Lumen Venou
Hazard: The Patient ID Card packaged with the POWERPORT ClearVUE Implantable Port with Smooth Septum contains incorrect port flushing instructions.
May 16, 2018Medical DevicesFDA
Bard Peripheral Vascular Inc recalls POWERPORT ClearVUE isp Implantable Port With Smooth Septum and Attachable 8F Polyurethane Open-Ended Single-Lumen Venous
Hazard: The Patient ID Card packaged with the POWERPORT ClearVUE Implantable Port with Smooth Septum contains incorrect port flushing instructions.
May 16, 2018Medical DevicesFDA
Bard Peripheral Vascular Inc recalls POWERPORT ClearVUE Slim with Smooth Septum, 8F ChronoFlex, Polyurethane Catheter with open suture holes, REF 5678301
Hazard: The Patient ID Card packaged with the POWERPORT ClearVUE Implantable Port with Smooth Septum contains incorrect port flushing instructions.
May 16, 2018Medical DevicesFDA
Bard Peripheral Vascular Inc recalls POWERPORT ClearVUE Slim with Smooth Septum, 8F ChronoFlex, Polyurethane Catheter with open suture holes, REF 5678300
Hazard: The Patient ID Card packaged with the POWERPORT ClearVUE Implantable Port with Smooth Septum contains incorrect port flushing instructions.
May 16, 2018Medical DevicesFDA
Bard Peripheral Vascular Inc recalls POWERPORT ClearVUE Slim with Smooth Septum, 6F ChronoFlex Silk, Polyurethane Catheter with Open Suture Holes, REF 567630
Hazard: The Patient ID Card packaged with the POWERPORT ClearVUE Implantable Port with Smooth Septum contains incorrect port flushing instructions.
May 16, 2018Medical DevicesFDA
Bard Peripheral Vascular Inc recalls POWERPORT ClearVUE Slim with Smooth Septum, 6F ChronoFlex Silk, Polyurethane Catheter, REF 5676300
Hazard: The Patient ID Card packaged with the POWERPORT ClearVUE Implantable Port with Smooth Septum contains incorrect port flushing instructions.
May 16, 2018Medical DevicesFDA
Bard Peripheral Vascular Inc recalls POWERPORT ClearVUE isp with Smooth Septum, 8F ChronoFlex, Polyurethane Catheter, REF 5668362
Hazard: The Patient ID Card packaged with the POWERPORT ClearVUE Implantable Port with Smooth Septum contains incorrect port flushing instructions.
May 16, 2018Medical DevicesFDA
Bard Peripheral Vascular Inc recalls POWERPORT ClearVUE isp with Smooth Septum, 6F ChronoFlex, Polyurethane Catheter, REF 5666362
Hazard: The Patient ID Card packaged with the POWERPORT ClearVUE Implantable Port with Smooth Septum contains incorrect port flushing instructions.
May 16, 2018Medical DevicesFDA
Bard Peripheral Vascular Inc recalls POWERPORT ClearVUE Slim with Smooth Septum, 8F ChronoFlex, Polyurethane Catheter with Open Suture Holes, REF 1678301
Hazard: The Patient ID Card packaged with the POWERPORT ClearVUE Implantable Port with Smooth Septum contains incorrect port flushing instructions.
May 16, 2018Medical DevicesFDA
Bard Peripheral Vascular Inc recalls POWERPORT ClearVUE Slim with Smooth Septum, 8F ChronoFlex, Polyurethane Catheter, REF 1678300
Hazard: The Patient ID Card packaged with the POWERPORT ClearVUE Implantable Port with Smooth Septum contains incorrect port flushing instructions.
May 16, 2018Medical DevicesFDA
Bard Peripheral Vascular Inc recalls POWERPORT ClearVUE Slim with Smooth Septum, 6F ChronoFlex, Polyurethane Catheter with Open Suture Holes, REF 1676301
Hazard: The Patient ID Card packaged with the POWERPORT ClearVUE Implantable Port with Smooth Septum contains incorrect port flushing instructions.
May 16, 2018Medical DevicesFDA
Bard Peripheral Vascular Inc recalls POWERPORT ClearVUE Slim with Smooth Septum, 6F ChronoFlex Silk, Polyurethane Catheter, REF 1676300
Hazard: The Patient ID Card packaged with the POWERPORT ClearVUE Implantable Port with Smooth Septum contains incorrect port flushing instructions.
May 16, 2018Medical DevicesFDA
Bard Peripheral Vascular Inc recalls POWERPORT ClearVUE isp with Smooth Septum, 8F ChronoFlex, Polyurethane Catheter, REF 1668362
Hazard: The Patient ID Card packaged with the POWERPORT ClearVUE Implantable Port with Smooth Septum contains incorrect port flushing instructions.
May 16, 2018Medical DevicesFDA
Bard Peripheral Vascular Inc recalls POWERPORT(R) ClearVUE(R) isp with Smooth Septum, 6F ChronoFlex(TM), Polyurethane Catheter, REF 1666362
Hazard: The Patient ID Card packaged with the POWERPORT ClearVUE Implantable Port with Smooth Septum contains incorrect port flushing instructions.
November 1, 2017Medical DevicesFDA
Bard Peripheral Vascular Inc recalls BARD MAX-CORE Disposable Core Biopsy Instrument, Product Codes - MC1410, 14 g x 10 cm; MC1616, 16 g x 16 cm; MC1816, 18
Hazard: During the review of May 2017 complaint data, a significant increase in MAX-CORE Disposable Core Biopsy Instrument complaints was observed for Failure to Prime, Failure to Fire, Failure to Obtain Sample, and Self-Activation.
May 10, 2017Medical DevicesFDA
Bard Peripheral Vascular Inc recalls MR GHIATAS Beaded Breast Localization Wire, Product Code: 477201, 479201 Product Usage: The GHIATAS Beaded Breast Lo
Hazard: It may be at risk of containing a non-MR compatible GHIATAS Beaded Breast Localization Wire instead of a MR compatible GHIATAS Beaded Breast Localization Wire.
January 25, 2017Medical DevicesFDA
BARD PERIPHERAL VASCULAR, INC recalls Halo One 5F Introducer Sheath 10 cm 5 pack Product Code: HAL510F Product Usage: The Halo One Thin-Walled Guiding Sh
Hazard: Complaints of sheath separation, kinking, and/or tip damage during use.
January 25, 2017Medical DevicesFDA
BARD PERIPHERAL VASCULAR, INC recalls Halo One 5F Introducer Sheath 90 cm Product Code: HAL590 Product Usage: The Halo One Thin-Walled Guiding Sheath i
Hazard: Complaints of sheath separation, kinking, and/or tip damage during use.
January 25, 2017Medical DevicesFDA
BARD PERIPHERAL VASCULAR, INC recalls Halo One 5F Introducer Sheath 45 cm Product Code: HAL545 The Halo One Thin-Walled Guiding Sheath is designed to perfor
Hazard: Complaints of sheath separation, kinking, and/or tip damage during use.