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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.
August 18, 2021Medical DevicesFDA
Bard Peripheral Vascular Inc recalls TIN3018 Illinois Bone Marrow Aspiration/Intraosseous Infusion Needle 18G x 79mm TIN3015 Illinois Bone Marrow Aspiration
Hazard: Due to complaints received regarding incomplete/open packaging seals potentially causing product to non-sterile.
August 18, 2021Medical DevicesFDA
Bard Peripheral Vascular Inc recalls EJM4011 Jamshidi Evolve" Bone Marrow Biopsy/Aspiration Needle with Specimen Cradle. 11G x 10cm
Hazard: Due to complaints received regarding incomplete/open packaging seals potentially causing product to non-sterile.
August 18, 2021Medical DevicesFDA
Bard Peripheral Vascular Inc recalls TJM6008 Jamshidi" Crown Bone Marrow Biopsy/Aspiration Needle with Marrow Acquisition Cradle. 8G x 15 cm; TJC3513 Jamshi
Hazard: Due to complaints received regarding incomplete/open packaging seals potentially causing product to non-sterile.
June 23, 2021Medical DevicesFDA
Bard Peripheral Vascular Inc recalls VENOVO Venous Stent System 9F Product Description(REF)/dimension: VENEL14040 /Venovo 9F 14/40/1200mm OUS; VENEL1406
Hazard: Reports of the proximal end of the stent not immediately expanding upon deployment and remaining connected to the delivery system.
June 23, 2021Medical DevicesFDA
Bard Peripheral Vascular Inc recalls VENOVO Venous Stent System 8F Product Description(REF)/dimension: VENEL10040 /Venovo 8F 10/40/1200mm OUS; VENEL1006
Hazard: Reports of the proximal end of the stent not immediately expanding upon deployment and remaining connected to the delivery system.
June 23, 2021Medical DevicesFDA
Bard Peripheral Vascular Inc recalls VENOVO Venous Stent System 10F Product Description(REF)/dimension: VENEL16040 Venovo 10F 16/40/1200mm OUS VENEL1606
Hazard: Reports of the proximal end of the stent not immediately expanding upon deployment and remaining connected to the delivery system.
May 19, 2021Medical DevicesFDA
Bard Peripheral Vascular Inc recalls PowerPort duo M.R.I. Implantable Port, with attachable 9.5F Polurethane Open-Ended Dual-Lumen Venous Catheter, REF 58295
Hazard: Catheters may experience difficulty in flushing, infusion, and/or aspiration, and septum dislodgements.
May 19, 2021Medical DevicesFDA
Bard Peripheral Vascular Inc recalls PowerPort duo M.R.I. Implantable Port, with attachable 9.5F Polurethane Open-Ended Dual-Lumen Venous Catheter, REF 18295
Hazard: Catheters may experience difficulty in flushing, infusion, and/or aspiration, and septum dislodgements.
May 19, 2021Medical DevicesFDA
Bard Peripheral Vascular Inc recalls PowerPort duo M.R.I. Implantable Port, with attachable 9.5F Polurethane Open-Ended Dual-Lumen Venous Catheter, REF 18295
Hazard: Catheters may experience difficulty in flushing, infusion, and/or aspiration, and septum dislodgements.
March 31, 2021Medical DevicesFDA
Bard Peripheral Vascular Inc recalls BARD MARQUEE Disposable Core Biopsy Instruments XX.Xcm, XX.Xcm, XXg x XXcm REF XXXXXXX Note - for definition of the
Hazard: Due to the Penetration Depth Switch used to select the desired penetration depth of the biopsy needle for soft tissue biopsies, detaches from the device during use.
October 14, 2020Medical DevicesFDA
Bard Peripheral Vascular Inc recalls Bard Conquest PTA Balloon dilation Catheter, 6mm x 40mm, 75 cm, Cat. No. CQ7564, UDI: (01) 00801741062902 - Product Usag
Hazard: Dilation catheter packaged with the wrong size balloon. The labeling states that the balloon size is 6mm x 40mm, however included is a 5mm x 40mm balloon. Use of a balloon that has a smaller diameter than expected could result in inconsequential prolongation of an existing procedure.
June 10, 2020Medical DevicesFDA
Bard Peripheral Vascular Inc recalls EQUISTREAM¿ XK Long-Term Hemodialysis Catheter. REF/UDI:5913190/(01)00801741013836; 16F
Hazard: Incorrect Peel-Apart Introducer Sheath in Kit.
June 10, 2020Medical DevicesFDA
Bard Peripheral Vascular Inc recalls EQUISTREAM¿ XK Long-Term Hemodialysis Catheter. REF/UDI:5913230/:(01)00801741013843; 16F
Hazard: Incorrect Peel-Apart Introducer Sheath in Kit.
May 20, 2020Medical DevicesFDA
Bard Peripheral Vascular Inc recalls BARD Access Systems PowerPort ClearVUE Slim Implantable Port With Smooth Septum and Attachable 6 F Polyurethane Open-End
Hazard: The catheter locks for the lot may contain an 8Fr catheter lock instead of a 6Fr catheter lock per device labeling.
April 15, 2020Medical DevicesFDA
Bard Peripheral Vascular Inc recalls Jamshidi Bone Marrow Biopsy/Aspiration Needle, with Luer Lock Adapter 11GX4 ASP, Sterile - Product Code: DJ4011X - Produ
Hazard: Sterility compromised due to packaging pouches that may not be sealed properly
April 8, 2020Medical DevicesFDA
Bard Peripheral Vascular Inc recalls BD WAVELINQ 4F EndoAVF System, Arterial Catheter 50 cm, Venous Catheter 43 cm, Sterile EO, Rx only, Mfr. Bard Peripheral
Hazard: The firm has become aware of a potential problem with their venous and arterial magnetic catheters may be at risk of experiencing a magnetic deficiency, which may result in the magnets failing to attract to one another. This may result in procedural delay in obtaining or creating a functional fistula and need for additional contrast to perform the necessary fluoroscopy. This can pose an incremental risk of harm to a diabetic patient's kidney function.
April 1, 2020Medical DevicesFDA
Bard Peripheral Vascular Inc recalls PowerFlow Implatable Apheresis IV Port with attachable 9.6 F ChronoFl x Open-Ended Single-Lumen Venous Catheter, Ref A7
Hazard: Firm has identified that the product may be at risk of incorrectly containing a tunneler with a barb tip meant to attach to a 6Fr catheter instead of the correct barb tip for a 9.6Fr catheter. This can result in a prolongation of operation.
April 1, 2020Medical DevicesFDA
Bard Peripheral Vascular Inc recalls 1. X-Port isp M.R.I Implantable Port, with Pre-Attached 9.6 F Open-Ended Single-Lumen Venous Catheter, REF:0607550, UDI:
Hazard: Firm has identified that the product may be at risk of incorrectly containing a tunneler with a barb tip meant to attach to a 6Fr catheter instead of the correct barb tip for a 9.6Fr catheter. This can result in a prolongation of operation.
April 1, 2020Medical DevicesFDA
Bard Peripheral Vascular Inc recalls BardPort M.R.I. Hard Base Implantable Port with Attachable 9.6 F Open-Ended Single-Lumen Venous Catheter, Ref: 0604550,
Hazard: Firm has identified that the product may be at risk of incorrectly containing a tunneler with a barb tip meant to attach to a 6Fr catheter instead of the correct barb tip for a 9.6Fr catheter. This can result in a prolongation of operation.
April 1, 2020Medical DevicesFDA
Bard Peripheral Vascular Inc recalls BardPort M.R.I. Implantable Port with Attachale 9.6 F Open-Ended Single-Lumen Venous Catheter, REF: 0602680, UDI:(01)008
Hazard: Firm has identified that the product may be at risk of incorrectly containing a tunneler with a barb tip meant to attach to a 6Fr catheter instead of the correct barb tip for a 9.6Fr catheter. This can result in a prolongation of operation.
April 1, 2020Medical DevicesFDA
Bard Peripheral Vascular Inc recalls BardPort Titanium Implantable Port with Attachable 9.6 F Open-Ended Single-Lumen Venous Catheter , REF: 0602230, UDI: (0
Hazard: Firm has identified that the product may be at risk of incorrectly containing a tunneler with a barb tip meant to attach to a 6Fr catheter instead of the correct barb tip for a 9.6Fr catheter. This can result in a prolongation of operation.
April 1, 2020Medical DevicesFDA
Bard Peripheral Vascular Inc recalls 1. Groshong 9.5 Dual-Lumen CV Catheter, Ref: 7726950, UDI: (01)00801741041570; 2. Groshong 9.5 F Dual-Lumen CV Cathete
Hazard: Firm has identified that the product may be at risk of incorrectly containing a tunneler with a barb tip meant to attach to a 6Fr catheter instead of the correct barb tip for a 9.6Fr catheter. This can result in a prolongation of operation.
April 1, 2020Medical DevicesFDA
Bard Peripheral Vascular Inc recalls 1. Vaccess CT Power-Injectable Implantable Port with Suture Plugs, Ref: 7496000, UDI:(01)00801741027482 Product Usage:
Hazard: Firm has identified that the product may be at risk of incorrectly containing a tunneler with a barb tip meant to attach to a 6Fr catheter instead of the correct barb tip for a 9.6Fr catheter. This can result in a prolongation of operation.
April 1, 2020Medical DevicesFDA
Bard Peripheral Vascular Inc recalls 1. Power Port isp M.R.I. Implantable Port with Attachable 9.6 F Open-Ended Single-Lumen Venous Catheter with Suture Plug
Hazard: Firm has identified that the product may be at risk of incorrectly containing a tunneler with a barb tip meant to attach to a 6Fr catheter instead of the correct barb tip for a 9.6Fr catheter. This can result in a prolongation of operation.
April 1, 2020Medical DevicesFDA
Bard Peripheral Vascular Inc recalls 1. PowerPort M.R.I. Implantable Port with Attachable 9.6 F Open-Ended Single-Lumen Venous Catheter with Suture Plugs, RE
Hazard: Firm has identified that the product may be at risk of incorrectly containing a tunneler with a barb tip meant to attach to a 6Fr catheter instead of the correct barb tip for a 9.6Fr catheter. This can result in a prolongation of operation.
April 1, 2020Medical DevicesFDA
Bard Peripheral Vascular Inc recalls 1.PowerPort Implantable Port With Attachable 9.6 F Open-Ended Single-Lumen Venous Catheter REF: 1709600, Air Guard, With
Hazard: Firm has identified that the product may be at risk of incorrectly containing a tunneler with a barb tip meant to attach to a 6Fr catheter instead of the correct barb tip for a 9.6Fr catheter. This can result in a prolongation of operation.
March 11, 2020Medical DevicesFDA
Bard Peripheral Vascular Inc recalls Bard Biopsy EnCor Probe, MRI, 10G Blunt Tip, REF number ECPMR0110GBT, packaged individually in sterile pouches, 5 pouche
Hazard: Lot numbers and products inadvertently not included in the scope of the previous recall. Original recall was conducted due to an increase in probe failures for leaks, suction issues, and failure to obtain samples.
March 11, 2020Medical DevicesFDA
Bard Peripheral Vascular Inc recalls Bard Biopsy EnCor Probe, MRI, 10G Trocar Tip, REF number ECPMR0110G, packaged individually in sterile pouches, 5 pouches
Hazard: Lot numbers and products inadvertently not included in the scope of the previous recall. Original recall was conducted due to an increase in probe failures for leaks, suction issues, and failure to obtain samples.
March 11, 2020Medical DevicesFDA
Bard Peripheral Vascular Inc recalls Bard Biopsy EnCor Probe, MRI, 7G Trocar Tip, REF number ECPMR017G, packaged individually in sterile pouches, 5 pouches/c
Hazard: Lot numbers and products inadvertently not included in the scope of the previous recall. Original recall was conducted due to an increase in probe failures for leaks, suction issues, and failure to obtain samples.
March 11, 2020Medical DevicesFDA
Bard Peripheral Vascular Inc recalls Bard Biopsy EnCor Probe, Stereotactic/Ultrasound 7G, REF number ECP017G, packaged individually in sterile pouches, 5 pou
Hazard: Lot numbers and products inadvertently not included in the scope of the previous recall. Original recall was conducted due to an increase in probe failures for leaks, suction issues, and failure to obtain samples.