Bard PowerPort Plaintiff Acquisition - Since 2009
Trust The Industry's Only Lead Replacement Guarantee and High-Tech Verification. C.R. Bard may have put thousands of patients at risk for complications ranging from internal lacerations to permanent damage. We provide Bard PowerPort lawsuit leads with documentation you can use.
Every qualified claimant arrives as a complete intake summary - case criteria, injury and timeline details, verification, agreements and supporting documents - ready for your intake team to review.
Only available on live transfer and signed retainer lead packages.
Delivery Options
Every docket is different. Choose the stage where you want mass tort claimants to land — or mix delivery types across torts as each litigation moves from early filings toward settlement.
Pre-screened claimants matched to your tort’s criteria — product, diagnosis and exposure window — delivered in real time and exclusive to your firm.
Best for: firms with in-house paralegals or intake staff that want volume across several active torts.
Our non-incentivized intake agents walk the claimant through your tort questionnaire by phone, then warm-transfer the call directly to your team.
Best for: firms that want a case manager speaking with every mass tort claimant first.
We handle qualification, documentation and signature on your firm’s retainer — the claimant arrives QC-reviewed with the full file attached.
Best for: firms that want signed claimants on the docket, not leads to chase.
Pricing is quoted per tort and depends on the litigation, its stage, your volume and how strict your criteria are.
Qualified leads are the middle of what we do, and the rest of this page covers them in detail. If you already know you want something further down the chain — claimants already signed onto your paper — that is a separate service, and you can skip straight to it.
Thousands May Be Entitled to Legal Remedies
Some of the largest mass torts today focus on medical devices like the C.R. Bard PowerPort that sailed through the FDA's accelerated 510(k) approval process. Instead of being stronger than other catheterization options as advertised, already chronically-ill patients suffered internal injuries as these devices failed. Injury Case Claims stands out among the numerous lead generation offerings because of our:
Our intake specialists are non-incentivized to maximize lead volume - only cases that end up as successfully signed retainers. Combined with stringent submission form requirements that match your criteria, you stay in control of your lawsuit leads.
All leads from Injury Case Claims are generated in compliance with ABA, GDPR, TCPA, and other regulations, ensuring high ethical and legal standards. Quality process means leads that come without issue.
We use advanced AI screening and biometrics as part of our identity confirmation process, reducing fraud and ensuring lead authenticity. When needed, we offer on-the-ground investigators to follow up claims far from your office.
With easy integration into most popular case management systems, our processes reduce administrative load with live transfers and retainer signing, streamlining intake for faster client engagement.
Injury Case Claims has extensive experience in plaintiff acquisition since 2009, delivering more than 60,000 qualified potential plaintiffs to law firm partners nationwide.
With KPIs and metrics you can analyze throughout the campaign, we make sure you are getting the maximum qualified leads no matter where we advertise. We take your investment seriously.
Key Things to Know
We focus on the following in our lead generation for Bard PowerPort cases. Understanding the demographics and case profile helps us deliver only the most qualified plaintiffs to your firm.
Best Practices
We follow proven best practices in our lead generation and intake process to ensure only the highest quality Bard PowerPort cases are delivered to your firm.
Practice #1
Unlike other medical records reviews, this provides the exact timeline and correlative link between the PowerPort and any injuries suffered. It is important to compare the dates of any complications with other plaintiffs' to detail how long it took for systems to fail in most patients, improving the causality link.
Practice #2
The PowerPort catheter system was supposed to be used in complex medical cases where it would be stronger than alternatives. Experts who can testify to its actual failure rate compared to advertised benefits will develop stronger cases.
Practice #3
If necessary, subpoena hospital protocols for internal records on what professionals performed when inserting or accessing the Bard device and how it compared to other port systems they may have used in the past.
Practice #4
While the recall was already initiated, collecting evidence of failures prior to its release can indicate that C.R. Bard knew or should have known about the risks regarding the device.
Practice #5
While it's rare for a defective medical device claim to coincide with a medical malpractice claim, if there were differences in usage based on Bard's implied promises, it can bolster a claim.
Get Started
Injury Case Claims is the only full-service lead generation for mass tort law firms that can take potential plaintiffs from inbound traffic to signed retainers - all with the guarantees of biometric identification and HIPAA-compliant transfer directly into your case management system.
Get Started
With a robust 7-day replacement guarantee for all leads to ensure they meet each of your standards, Injury Case Claims is your partner for Bard PowerPort lawsuit leads.
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FAQ
Everything you need to know about our Bard PowerPort lawsuit leads, pricing, and guarantees.