Bard PowerPort Leads
Connect with patients who experienced device fracture, migration, embolism, or serious infection from Bard PowerPort implantable port catheter devices.
Bard PowerPort Device Litigation
The Bard PowerPort is an implantable port catheter device used to deliver medications, fluids, and blood products directly into the bloodstream, commonly used by cancer patients undergoing chemotherapy. Reports indicate these devices are prone to fracture, catheter migration, and other mechanical failures that can lead to life-threatening complications including pulmonary embolism. Lawsuits allege Bard (now part of BD) manufactured defective devices and failed to warn about the risks of device failure.
Associated Conditions
- Device fracture and catheter breakage
- Catheter migration to the heart or lungs
- Pulmonary embolism
- Infection at the port site or bloodstream
- Blood clots and deep vein thrombosis
- Cardiac arrhythmia or perforation
- Need for surgical removal or revision
Claimant Eligibility
- Had a Bard PowerPort device implanted
- Experienced device fracture, migration, or mechanical failure
- Required emergency surgery or hospitalization due to device complications
- Diagnosed with embolism, infection, or thrombosis related to the device
- Medical records documenting the device implantation and complications
Why Law Firms Choose Us
Exclusive Leads
Every lead is yours alone. We never resell or share claimant information with competing firms, guaranteeing you first-mover advantage on every case.
Pre-Qualified Claimants
Our intake specialists screen every potential claimant against your specific case criteria before delivery, so your team only speaks with viable cases.
Live Transfer
Qualified claimants are transferred directly to your intake team in real time, maximizing conversion rates and reducing time-to-retainer.
Ready to Scale Your Mass Tort Practice?
Tell us about your firm and a mass tort strategist will reach out within one business day.
Trusted by 200+ law firms nationwide