Bard Peripheral Vascular Inc recalls
Every recall we track for Bard Peripheral Vascular Inc — 117 in all, from 2017–2026 — plus the complaints and injury reports the public filed about them. 3 are rated “stop using now”.
Recalls per year, by danger level
Recalls from Bard Peripheral Vascular Inc peaked in 2019 (51); 117 since 2017. 3% rated “stop using now”.
All FDA recall records for Bard Peripheral Vascular Inc since 2017, counted by recall date (one bar per calendar year; 2026 is partial). Danger level is GovInfoNow’s plain-language rating; “not yet rated” records are still being written up.
| Year | Stop using now | Use caution | Lower risk | Not yet rated | Total |
|---|---|---|---|---|---|
| 2017 | 0 | 1 | 0 | 0 | 1 |
| 2018 | 0 | 0 | 17 | 0 | 17 |
| 2019 | 0 | 34 | 17 | 0 | 51 |
| 2020 | 0 | 0 | 10 | 0 | 10 |
| 2021 | 1 | 4 | 5 | 0 | 10 |
| 2022 | 1 | 9 | 2 | 1 | 13 |
| 2023 | 0 | 2 | 4 | 0 | 6 |
| 2024 | 1 | 2 | 1 | 0 | 4 |
| 2025 | 0 | 2 | 2 | 0 | 4 |
| 2026 (to date) | 0 | 1 | 0 | 0 | 1 |
Most common reasons for Bard Peripheral Vascular Inc recalls
What to do if you have a recalled Bard Peripheral Vascular Inc product
- Match the model, catalog or lot number on your device to the recall.
- Ask the prescribing clinician or supplier what to do — many device recalls are corrections, not removals.
- Report problems to FDA MedWatch.
All Bard Peripheral Vascular Inc recalls
41 shown- Use cautionMedical device
Bard Peripheral Vascular Inc recalls EnCor EnCompass Breast Biopsy and Tissue Removal System Console (model number: ENCPCONSOLE) and Driver (model number:
Bard Peripheral Vascular Inc recalls EnCor EnCompass Breast Biopsy and Tissue Removal System Console and Driver with specific software versions and serial numbers due to potential calibration errors that could interrupt procedures or require repeat biopsies.
Bard Peripheral VascularAug 20, 2026 - Lower riskMedical device
Bard Peripheral Vascular Inc recalls Broviac 4.2 Fr Single-Lumen CV Catheter Cutdown Tray with SureCuff Tissue Ingrowth Cuff Cat 60060
Bard recalls specific Broviac and Hickman catheter cutdown trays with SureCuff cuffs due to potential damage to the outer tray that could compromise the sterile barrier. Affected products include various sizes and models with catalog numbers 600060-606560.
BardDec 12, 2025 - Use cautionMedical device
Bard Peripheral Vascular Inc recalls Safe-T-Centesis 6 Fr Catheter Drainage Tray, REF: PIG1260T,
Bard recalls Safe-T-Centesis 6 Fr Catheter Drainage Tray (REF: PIG1260T) due to safety indicators that may show catheter in sharp position when it's blunt, risking internal injury or delayed treatment.
BardNov 6, 2025 - Lower riskMedical device
Bard Peripheral Vascular Inc recalls Venclose digiRF Generators, Model VCRFG1, with software 3.35 designed to identify internal wiring anomalies in the
Bard recalls Venclose digiRF Generators (Model VCRFG1) with software 3.35 that may falsely flag Venclose EVSRF Ablation Catheters as defective due to temperature issues during verification.
BardAug 21, 2025 - Use cautionMedical device
Bard Peripheral Vascular Inc recalls Rotarex Atherectomy System and Instructions for Use, BD SET Rotarex: S 6 F x 110 cm, REF: 80236; S 6 F x 135 cm, REF:
Bard recalls Rotarex Atherectomy Systems with specific model numbers due to risk of catheter breakage causing vessel injury and severe bleeding during medical procedures.
BardFeb 5, 2025 - Use cautionMedical device
Bard Peripheral Vascular Inc recalls Bard Marquee Disposable Core Biopsy Instrument Kit: BARD MARQUEE KIT 12G X 10 CM, REF: MQK1210; BARD MARQUEE 12G X 10
Bard recalls Marquee disposable biopsy kits with potential missing needle retention notch. This could cause needle detachment, tissue damage, or bleeding during medical procedures. Affected kits include specific model numbers and expiration dates.
BardSep 30, 2024 - Stop using nowMedical device
Bard Peripheral Vascular Inc recalls The EVSRF catheter is a sterile, single-use disposable medical device for endovenous radiofrequency ablation, a
Bard Peripheral Vascular recalls EVSRF catheters with internal wiring errors that cause overheating. Affected units have swapped red/yellow signal wires, risking burns and tissue damage during radiofrequency ablation procedures.
Bard Peripheral VascularSep 4, 2024 - Lower riskMedical device
Bard Peripheral Vascular Inc recalls BARD MAGNUM Disposable Core Tissue Biopsy Needle REF: MN1410 MN 1420 MN1610 MN1616 MN1820 MN2010 The Magnum Biopsy
Bard recalls Magnum Disposable Core Tissue Biopsy Needles (models MN1410-MN2010) due to possible packaging damage that could compromise sterile barrier. Affected users should check product labels for specific model numbers and lot codes.
BardAug 2, 2024 - Use cautionMedical device
Bard Peripheral Vascular Inc recalls Guidewire 70cm x 1mm (0.038 ) REF 5583705 These accessories are intended for use with Bard 14.5 Fr. Long-Term Dual
Bard recalls specific guidewires that may be misassembled, causing injury if inserted incorrectly. Affected units include REF 5583705 with certain lot numbers.
BardJul 10, 2024 - Use cautionMedical device
Bard Peripheral Vascular Inc recalls BD Recanalization System, REF: BDRECANSYSTEM
Bard recalls specific recanalization systems that may run continuously without required pauses, increasing risk of overheating or breaking. Affected units have serial numbers starting with BSX000001 to BSX000444.
BardNov 14, 2023 - Lower riskMedical device
Bard Peripheral Vascular Inc recalls Bard Mission Disposable Core Biopsy Instrument Kit (REF/Name): 1410MSK/ Mission Kit 14G x 10CM; 1416MSK/ Mission Kit
Bard Peripheral Vascular Inc product list for medical devices. Includes a comprehensive list of products with their corresponding model numbers and dates.
Bard Peripheral Vascular IncNov 8, 2023 - Use cautionMedical device
Bard Peripheral Vascular Inc recalls Bard Marquee Disposable Core Biopsy Instrument Kit, REF: MQK2016
Bard recalls Marquee Disposable Core Biopsy Instrument Kit REF: MQK2016 due to diameter mismatch causing improper needle fit, potential pain, pneumothorax, or bleeding during procedures.
BardAug 10, 2023 - Lower riskMedical device
Bard Peripheral Vascular Inc recalls Bard Mission Disposable Core Biopsy Instrument Kit: REF: 2010MSK, 20G x 10CM; REF: 2016MSK, 20G x 16CM
Bard recalls disposable core biopsy kits with specific model numbers due to potential procedure delays or repeat procedures from improper needle fitting.
BardApr 11, 2023 - Lower riskMedical device
Bard Peripheral Vascular Inc recalls Bard Mission Disposable Core Biopsy Instrument Kit: 16G x 10CM, REF: 1610MSK; 18G x 16CM, REF: 1816MSK
Bard recalls specific disposable core biopsy instrument kits due to potential needle tip breakage when used with incompatible instruments, which may require additional devices or cause procedural delays.
BardFeb 28, 2023 - Lower riskMedical device
Bard Peripheral Vascular Inc recalls Catalog Number / Product Description 0601600 2.7F Broviac CV Catheter Repair Kit 0601610 4.2 Fr Broviac CV Catheter
Bard recalls specific Broviac CV catheter repair kits due to potential hardened adhesive that could be unusable. Affected kits include various sizes and model numbers with specific lot/serial codes.
BardJan 4, 2023 - Use cautionMedical device
Bard Peripheral Vascular Inc recalls The Covera Vascular Covered Stent is a flexible, self-expanding endoprothesis comprised of ePTFE encapsulating a
Bard Peripheral Vascular recalls specific models of Covera Vascular Covered Stents due to reported inability to deploy, linked to poor slide block bonding. Affected units have unique catalog numbers and UDI codes listed in the recall.
Bard Peripheral VascularDec 22, 2022 - Use cautionMedical device
Bard Peripheral Vascular Inc recalls REF: PIG1260K, 6Fr, X10, Safe-t-Centesis Catheter drainage Kit, Sterile EO,
Bard recalls Safe-t-Centesis Catheter drainage kits with potential 8 Fr needle instead of 6 Fr. This could cause injury during use. Check your kit's lot number for recall.
BardApr 22, 2022 - Use cautionMedical device
Bard Peripheral Vascular Inc recalls LUMBAR PUNCTURE TRAY PEDIATRIC 21G 2.5
Bard recalls pediatric lumbar puncture trays with potential manometer leaks. Affected units have specific lot numbers; stop using immediately to prevent injury.
BardJan 20, 2022 - Lower riskMedical device
Bard Peripheral Vascular Inc recalls Catalog # BEK4511, Qty: 10, Ecomomy Jamshidi Bone Marrow Biopsy and Aspiration Tray, 11 G X 4"Biopsy/Aspiration needle,
Bard recalls 10 units of misbranded bone marrow biopsy trays and needles due to incorrect labeling. Affected items may not be safe for medical use without proper identification.
BardAug 24, 2021 - Use cautionMedical device
Bard Peripheral Vascular Inc recalls REF TIN3015, 15G x 79 mm Bone Marrow Aspiration/Intraosseous Infusion Needle, For Single Use Only, Sterile EO, UDI:
Bard recalls 15G x 79 mm Bone Marrow Aspiration/Intraosseous Infusion Needles (REF TIN3015) with potential for needle protector to dislodge, causing needle stick injuries.
BardJul 27, 2021 - Lower riskMedical device
Bard Peripheral Vascular Inc recalls TJM6008 Jamshidi" Crown Bone Marrow Biopsy/Aspiration Needle with Marrow Acquisition Cradle. 8G x 15 cm; TJC3513
Bard recalls Jamshidi bone marrow biopsy needles due to incomplete packaging seals that may allow non-sterile product. Affected models include TJM6008 and TJC3513. Consumers should check serial numbers and contact Bard for details.
BardJun 23, 2021 - Use cautionMedical device
Bard Peripheral Vascular Inc recalls PowerPort duo M.R.I. Implantable Port, with attachable 9.5F Polurethane Open-Ended Dual-Lumen Venous Catheter, REF
Bard recalls PowerPort duo M.R.I. Implantable Port systems with potential catheter flushing and infusion problems. Affected units may have septum dislodgements.
BardMar 25, 2021 - Use cautionMedical device
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
Bard recalls disposable core biopsy instruments with a penetration depth switch that can detach during use, posing a risk of injury. Affected models include MQ1210 to MQK2016 with specific UDI codes and lot numbers.
BardJan 14, 2021 - Lower riskMedical device
Bard Peripheral Vascular Inc recalls VENOVO Venous Stent System 9F Product Description(REF)/dimension: VENEL14040 /Venovo 9F 14/40/1200mm OUS; VENEL14060
Bard Peripheral Vascular Inc recalls VENOVO Venous Stent System 9F models with serial numbers starting with ANE... due to reports of stent not expanding immediately after deployment and remaining connected to delivery system. Affected units include specific model codes and serial numbers listed in the recall notice.
Bard Peripheral Vascular IncDec 14, 2020 - Lower riskMedical device
Bard Peripheral Vascular Inc recalls Bard Conquest PTA Balloon dilation Catheter, 6mm x 40mm, 75 cm, Cat. No. CQ7564, UDI: (01) 00801741062902 - Product
Bard recalls Conquest PTA Balloon dilation Catheter (6mm x 40mm) due to incorrect balloon size. Using a smaller balloon may prolong procedures without serious injury risk.
BardOct 1, 2020 - Lower riskMedical device
Bard Peripheral Vascular Inc recalls Jamshidi Bone Marrow Biopsy/Aspiration Needle, with Luer Lock Adapter 11GX4 ASP, Sterile - Product Code: DJ4011X -
Bard recalls sterile bone marrow biopsy needles (product code DJ4011X) due to potential packaging pouch leaks causing sterility issues. Affected lots 0001303256 and 0001303257.
BardMar 17, 2020 - Lower riskMedical device
Bard Peripheral Vascular Inc recalls BARD Access Systems PowerPort ClearVUE Slim Implantable Port With Smooth Septum and Attachable 6 F Polyurethane
Bard recalls PowerPort ClearVUE Slim implantable ports with possible wrong catheter lock size. Affected units may cause complications if used incorrectly. Contact Bard for details.
Bard Peripheral VascularJan 15, 2020 - Lower riskMedical device
Bard Peripheral Vascular Inc recalls Bard Biopsy EnCor Probe, MRI, 10G Trocar Tip, REF number ECPMR0110G, packaged individually in sterile pouches, 5
Bard recalls MRI-compatible 10G trocar tips due to past probe failures causing leaks, suction problems, and sample collection issues. Affected units have specific lot numbers and packaging.
BardJan 3, 2020 - Lower riskMedical device
Bard Peripheral Vascular Inc recalls BARD MAX-CORE Disposable Core Biopsy Instrument - Product Usage: The core needle biopsy device is intended for use in
Bard recalls MAX-CORE Disposable Core Biopsy Instruments with failure to fire and sample issues. These devices are used for soft tissue biopsies. Check product codes and serial numbers for affected units.
BardOct 25, 2019 - Lower riskMedical device
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,
Bard recalls specific implantable ports that may contain incorrect catheter tips, potentially prolonging surgery. Affected units include those with reference number 0604550 and lot number RECR1431.
BardOct 1, 2019 - Lower riskMedical device
Bard Peripheral Vascular Inc recalls Bard Conquest 40 PTA Dilation Catheter, 8mm X 20mm x 75cm (CQF7582), 8mm x 40mm x 75cm (CQF7584); Recommended Guidewire
Bard recalls specific 40 PTA Dilation Catheters due to incorrect balloon size labeling, which may cause injury during dialysis procedures. Affected units have a risk of non-diseased vessel dilation.
BardAug 14, 2019 - Use cautionMedical device
Bard Peripheral Vascular Inc recalls EQUISTREAM¿ XK Long-Term Hemodialysis Catheter. REF/UDI:5913190/(01)00801741013836; 16F
Bard recalls EQUISTREAM XK Long-Term Hemodialysis Catheters with incorrect peel-apart introducer sheath. This may cause complications during dialysis procedures. Affected units have specific model and serial numbers.
BardJun 14, 2019 - Use cautionMedical device
Bard Peripheral Vascular Inc recalls GlidePath Long-Term Hemodialysis Catheter with Preloaded stylet, REF/Product code:5397270, 14.5F, straight, 27cm
Bard recalls GlidePath long-term hemodialysis catheters with preloaded stylet (model 5397270) due to tunneler tip breaking during placement, potentially causing complications. Affected units have specific lot numbers and expiration dates.
BardMay 31, 2019 - Lower riskMedical device
Bard Peripheral Vascular Inc recalls EnCor Breast Biopsy Probes, packaged individually in sterile pouches, 5 pouches/carton, single use, Rx, catalog/REF
Bard recalls EnCor Breast Biopsy Probes with leaks and suction problems. Affected units have specific lot numbers. Stop using if you have these probes.
BardMay 2, 2019 - Use cautionMedical device
Bard Peripheral Vascular Inc recalls BD WAVELINQ 4F EndoAVF System, Arterial Catheter 50 cm, Venous Catheter 43 cm, Sterile EO, Rx only, Mfr. Bard
Bard recalls WavelinQ 4F EndoAVF System due to potential magnetic deficiency in catheters, which may cause procedural delays and increased kidney risk for diabetic dialysis patients. Affected units include specific model and lot numbers.
BardApr 12, 2019 - Use cautionMedical device
Bard Peripheral Vascular Inc recalls LIFESTREAM Balloon Expandable Vascular Covered Stent . BARD PERIPHERAL VASCULAR. 6mm X 26mm X 80 Recommended Introducer
Bard Peripheral Vascular recalls LIFESTREAM balloon expandable vascular stents with specific lot numbers due to potential issues when used with 6F introducer sheaths, which may cause insertion difficulties.
Bard Peripheral VascularFeb 18, 2019 - Lower riskMedical device
Bard Peripheral Vascular Inc recalls PowerPort isp M.R.I. Implantable Port with Attachable 8F Polyurethane Open-Ended Single-Lumen Venous Catheter
Bard recalls PowerPort isp MRI implantable ports with incorrect introducer sheath size. Affected units may cause complications during procedures. Contact Bard for details.
BardFeb 14, 2019 - Lower riskMedical device
Bard Peripheral Vascular Inc recalls POWERPORT CLEARVUE isp, 6F CHRONOFLEX Catheter, Intermediate NAUTILUS DELTA Kit; POWERPORT CLEARVUE isp, 8F CHRONOFLEX
Bard recalls specific POWERPORT CLEARVUE catheter and NAUTILUS DELTA kit models that may cause loss of ECG signal during port placement procedures. Affected units include certain product codes and lot numbers.
BardJun 25, 2018 - Lower riskMedical device
Bard Peripheral Vascular Inc recalls BARD PERIPHERAL VASCULAR SEEKER(R) Crossing Support Catheter, 0.035", 150 cm, REF SK15035M. Intended to support a
Bard Peripheral Vascular recalls Seeker Crossing Support Catheters (0.035" x 150cm) due to potential bacterial endotoxin cross-contamination in packaging. Affected units have UDI (01)00801741067921(17)191115(10)VTBY0563. Contact for remedy.
Bard Peripheral VascularApr 16, 2018 - Lower riskMedical device
Bard Peripheral Vascular Inc recalls POWERPORT ClearVUE isp with Smooth Septum, 6F ChronoFlex, Polyurethane Catheter, REF 5666362
Bard recalls POWERPORT ClearVUE implantable ports with incorrect flushing instructions that could lead to improper use. Affected units have specific lot numbers and reference codes.
BardFeb 8, 2018 - Use cautionMedical device
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
Bard recalls MAX-CORE Disposable Core Biopsy Instruments with specific model codes due to increased complaints of failure to prime, fire, obtain samples, or self-activation.
BardSep 22, 2017
Bard Peripheral Vascular Inc recall questions
How many recalls has Bard Peripheral Vascular Inc had?
117 recalls from Bard Peripheral Vascular Inc are on record with U.S. safety agencies, from 2017–2026.
What is the most recent Bard Peripheral Vascular Inc recall?
Bard Peripheral Vascular Inc recalls EnCor EnCompass Breast Biopsy and Tissue Removal System Console (model number: ENCPCONSOLE) and Driver (model number:, dated Aug 20, 2026. Every Bard Peripheral Vascular Inc recall is listed on this page, newest first.
Why are Bard Peripheral Vascular Inc products recalled?
The most common reasons on record: Due to lumbar puncture tray manometer failure mode of leaking and mating issues. (11); Due to misbranded products shipped to customers. (2); Incorrect Peel-Apart Introducer Sheath in Kit. (2).
What should I do if I have a recalled Bard Peripheral Vascular Inc product?
Match the model, catalog or lot number on your device to the recall. Ask the prescribing clinician or supplier what to do — many device recalls are corrections, not removals. Report problems to FDA MedWatch.
How do I get alerts for new Bard Peripheral Vascular Inc recalls?
Sign up for free email alerts on GovInfoNow — we check official CPSC, FDA, USDA and NHTSA data every day and email you only when a recall matches what you follow.