Every recall we track for Bard Peripheral Vascular Inc — 116 in all — plus the complaints and injury reports the public filed about them.
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.
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.
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.
Bard recalls Rotarex Atherectomy Systems with specific model numbers due to risk of catheter breakage causing vessel injury and severe bleeding during medical procedures.
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.
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 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.
Bard recalls specific guidewires that may be misassembled, causing injury if inserted incorrectly. Affected units include REF 5583705 with certain lot numbers.
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.
Bard Peripheral Vascular Inc product list for medical devices. Includes a comprehensive list of products with their corresponding model numbers and dates.
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.
Bard recalls disposable core biopsy kits with specific model numbers due to potential procedure delays or repeat procedures from improper needle fitting.
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.
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.
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 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.
Bard recalls Safe-T PLUS Pediatric Lumbar Puncture Trays with manometer leaks that could cause inaccurate spinal needle pressure readings during medical procedures.
Bard recalls adult 22G X3.5 Strel lumbar puncture trays due to manometer leaks and mating issues. Affected units have specific lot numbers. Stop using immediately to prevent potential complications.
Bard recalls adult lumbar puncture trays with potential manometer leaks. These medical devices may leak during procedures, causing inaccurate readings. Affected units have specific lot numbers and catalog IDs.
Bard recalls adult lumbar puncture trays with manometer leaks that could cause injury during medical procedures. Affected units have specific lot numbers and catalog codes.
Bard recalls adult lumbar puncture trays with manometer leaks that could cause inaccurate pressure readings during spinal procedures.
Bard recalls adult lumbar puncture drug-free trays with potential leaking and mating issues. Affected units have specific catalog numbers and lot numbers. Consumers should contact Bard for details.
Bard recalls adult lumbar puncture trays with model 4303C that may leak due to manometer failure. Affected units have specific lot numbers. Stop using immediately to prevent injury.
Bard recalls LUMBAR PUNCTURE DRUG FREE TRAY 22G due to manometer leaks that could cause injury during medical procedures. Affected units have specific lot numbers and catalog codes.
Bard recalls adult lumbar puncture trays with manometer leaks that could cause inaccurate pressure readings during spinal procedures.
Bard recalls specific SAFE-T PLUS ATRAUMATIC ADULT LP TRAYS due to manometer leaks. Affected units have unique lot numbers; stop using immediately to prevent injury.
Bard recalls pediatric lumbar puncture trays with potential manometer leaks. Affected units have specific lot numbers; stop using immediately to prevent injury.
Bard recalls misbranded Ecomomy Jamshidi Bone Marrow Biopsy Trays (Catalog # BEK3411) due to shipping errors. This affects medical devices used for bone marrow aspiration in life-threatening emergencies.
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.
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.
Bard recalls two bone marrow aspiration needles due to incomplete packaging seals that may allow non-sterile product. Affected units have specific serial numbers and catalog codes.
Bard recalls Jamshidi Evolve bone marrow biopsy needles with potential non-sterile packaging seals. Affected units may pose infection risk if used improperly.
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.
Bard recalls PowerPort duo M.R.I. Implantable Port systems with potential catheter flushing and aspiration issues that may cause septum dislodgement. Affected units have specific reference numbers.
Bard recalls PowerPort duo M.R.I. Implantable Port systems with potential catheter flushing and infusion problems. Affected units may need replacement to prevent complications.
Bard recalls PowerPort duo M.R.I. Implantable Port systems with potential catheter flushing and infusion problems. Affected units may have septum dislodgements.
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.
Bard is recalling VENOVO Venous Stent Systems 10F models with serial numbers listed in the notice due to reports of the stent not expanding properly after deployment, which could cause complications during medical procedures.
Bard Peripheral Vascular Inc recalls VENOVO Venous Stent Systems 8F models with serial numbers starting with ANEQ or ANDU. The stent may not expand properly after deployment, potentially causing complications. Affected units include specific model codes and serial numbers listed in the recall.
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 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.
Bard recalls sterile bone marrow biopsy needles (product code DJ4011X) due to potential packaging pouch leaks causing sterility issues. Affected lots 0001303256 and 0001303257.
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 recalls MRI-compatible 10G Biopsy Probes with potential leak or suction problems. Affected units have specific lot numbers and sterile packaging. Contact Bard for details.
Bard recalls specific MRI-compatible biopsy probes due to potential leaks and suction issues in certain lot numbers. Affected units include VTCT0272 and VTCV038: 5 pouches per carton.
Bard recalls specific models of biopsy probes due to increased failures like leaks and suction issues. Affected units include lot numbers VTCT0268-0271 and VTCU0340-0341.
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.
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.
Bard recalls two types of 9.5mm dual-lumen catheters that may contain incorrect barb tips, potentially prolonging medical procedures. Affected units have specific reference and lot numbers.
Bard recalls PowerPort M.R.I. Implantable Ports with 9.6F catheters that may contain incorrect barb tips, potentially prolonging surgery. Affected units have specific reference numbers and lot numbers.
Bard recalls 1. Vaccess CT Power-Injectable Implantable Ports with specific lot numbers due to risk of incorrect catheter tip causing surgery delays. Affected patients should contact Bard for details.
Bard recalls PowerPort implantable ports with 9.6F catheters that may have incorrect barb tips causing prolonged surgery. Affected units include specific model numbers and lot numbers.
Bard recalls PowerPort MRI implantable ports with potential incorrect catheter attachment causing prolonged surgery. Affected models include specific reference numbers and lot codes. Contact Bard for details.
Bard recalls titanium implantable ports with a risk of using wrong catheter tip causing prolonged surgery. Affected units have specific reference numbers. Contact Bard for details.
Bard recalls MRI implantable ports with 9.6F catheters that may have wrong tunneler tip, risking longer surgery. Affected units include specific lot numbers.
Bard recalls PowerFlow implantable apheresis ports with 9.6F catheters that may contain wrong catheter tips, causing prolonged procedures. Affected patients should contact Bard for details.
Bard recalls X-Port MRI implantable ports with specific catheter models due to risk of incorrect catheter tip causing prolonged surgery. Affected units have unique reference numbers and lots.
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.
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.
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 lot numbers and model details.
