Bard PowerPort MDL: Fracture Case Heads to Trial August 18
After a split first verdict, the Bard PowerPort MDL's second bellwether — a catheter fracture case — goes to trial August 18, 2026, with 3,376 cases pending.

Bard PowerPort MDL: Fracture Case Heads to Trial August 18

Shere Saidon
Shere Saidon

CEO & Founder at LlamaLab

Published July 8, 2026
7 min read
Mass Tort News

Bard PowerPort Litigation Shifts to Fracture Cases as Second Bellwether Nears

The second bellwether trial in the Bard PowerPort MDL will begin August 18, 2026 in the District of Arizona — a catheter fracture case brought by plaintiff Kimberly Divelbliss, according to a May 19 case management order. The trial follows a split outcome in the litigation's first test case: in early May 2026, the jury in Cook v. Becton Dickinson cleared Bard on failure-to-warn and consumer fraud claims but hung on the central design-defect question, leaving the MDL's core theory unresolved.

The stakes are substantial. MDL 3081 holds 3,376 pending cases alleging that Bard's implantable port catheters — used primarily by cancer patients receiving chemotherapy — are prone to fracture, migration, and infection. Judge David G. Campbell also reduced the planned bellwether trials from six to five in the same May 19 order, finding the remaining cases "will provide a meaningful and representative test of the claims and defenses."

3,376cases

Pending in MDL 3081 as of June 2026

5,333+

FDA adverse event reports for PowerPort catheters

Aug 182026

Second bellwether trial — a catheter fracture case

The First Verdict Was a Split Decision, Not a Sweep

Media coverage framed Cook as a defense win, but the verdict was narrower than the headlines. Plaintiff Robert Cook, a Minnesota colorectal cancer patient, alleged his PowerPort became infected, hospitalizing him for six days and delaying chemotherapy by two weeks. His counsel argued Bard knew for decades its devices were prone to infection yet shelved safer technologies — antimicrobial coatings, non-fouling surfaces, smoother catheter materials — developed as early as 2005.

What the Cook Jury Decided

  • Defense verdict on failure-to-warn
  • Defense verdict on failure-to-instruct
  • Defense verdict on consumer fraud
  • Jury cleared both Bard and parent Becton Dickinson on decided claims

What Remains Unresolved

  • The central design-defect claim hung — no unanimous verdict
  • Whether barium sulfate in the catheter material degrades device integrity
  • How juries will react to fracture and migration evidence (Cook was an infection case)
  • Judge Campbell had denied nearly all of Bard's summary judgment motion on March 5 — the claims survived to trial

The early read among litigation analysts: infection cases may be harder for plaintiffs than fracture or migration cases, because defendants can point to the patient's underlying condition — active cancer, immune suppression — as an alternative cause. Fracture cases come with an X-ray showing a broken catheter. That makes the August 18 Divelbliss trial a genuinely different test.

The Trial Schedule Through Early 2027

Bard PowerPort Bellwether Lineup

Trial DateCase Type
Status
April 21 – May 2026Infection (Cook v. Becton Dickinson)
Defense verdict on decided claims; design-defect claim hung
August 18, 2026Catheter fracture (Divelbliss)
Scheduled — second bellwether
October 13, 2026Bellwether #3
Scheduled
December 1, 2026Bellwether #4
Scheduled
February 2, 2027Bellwether #5
Scheduled

Judge Campbell has signaled that cases not resolved by settlement after these bellwethers will be transferred or remanded to their home districts for individual trials — the same playbook he ran in the earlier Bard IVC filter MDL. Industry commentators project per-case values in the $10,000 to $300,000+ range depending on injury severity, though no settlement framework exists yet.

Important

Why Case-Type Triage Now Drives Value

After Cook, firms are re-sorting inventories by injury type. Fracture and migration cases with clear imaging are moving to the front; infection cases need stronger causation workups connecting the device — not the patient's condition — to the injury. The August fracture trial will show whether that hierarchy holds.

Building the PowerPort Case File

PowerPort cases live and die on device identification and imaging. Not every port is a Bard port — the threshold question is whether the operative report names a Bard PowerPort, PowerPort isp, PowerPort MRI, ClearVUE, or related Bard device. From there, the injury must be documented, not inferred.

1

Confirm the device

Pull the implant operative report showing manufacturer, model, and serial number. Hospital billing records and device registration cards corroborate when the operative report is ambiguous.

2

Document the failure

X-ray, CT, or fluoroscopy showing catheter fracture, a migrated fragment, or the catheter out of position is the strongest single piece of proof in these cases.

3

Capture the treatment

Retrieval or explant surgical reports, interventional radiology notes, infection cultures and infectious disease consults, and records for any DVT, pulmonary embolism, or cardiac complication.

4

Anchor the timeline

Oncology records establish why the port was placed and how the failure disrupted treatment — Cook's two-week chemotherapy delay was central to his damages case.

The practical problem is that this evidence sits across three or four different provider systems: the implanting surgeon, the imaging center, the hospital that handled the failure, and the oncology practice. Firms working up PowerPort inventories ahead of the August trial are compressing that retrieval cycle — same-day retrieval services like LlamaLab pull operative reports, imaging, and treatment records from all providers in 24-48 hours, and flag the device identification buried inside operative reports so triage doesn't wait on a paralegal read-through.

What's Next

Key Points

Essential takeaways from this article

August 18, 2026: Divelbliss fracture trial — the first jury test of a fracture claim
October 13 and December 1, 2026, and February 2, 2027: three more bellwethers follow
A plaintiff verdict in a fracture case would reset settlement leverage after the split Cook outcome
Cases not resolved after the bellwethers face remand to home districts for individual trials
Statute of limitations: generally 2-4 years from discovery of the device-related injury, varying by state

The Bottom Line

The PowerPort MDL is entering its decisive stretch. One jury has already shown that infection claims face headwinds; the next four trials — starting with a fracture case on August 18 — will determine whether the litigation resolves globally or fragments into thousands of remanded trials.

For firms, the mandate is triage: sort inventories by injury type, confirm Bard device identification in every file, and close imaging gaps before the fall trials reshape the settlement math.

Triaging PowerPort Cases?

LlamaLab retrieves implant operative reports, imaging, and explant records from every provider in 24-48 hours — so you can classify fracture, migration, and infection cases before the August bellwether.


Sources: AboutLawsuits — Second Bellwether Order, MDL Update — MDL 3081, Verus — First Bellwether Verdict, Lawsuit Legal — Qualification Criteria, Harm Report — Case Documentation. Case counts current as of June 2026.

This article provides general information about Bard PowerPort litigation developments and should not be construed as legal or medical advice. Consult with qualified professionals for advice specific to your situation.

Stay Updated with Latest Insights

Get the latest articles about medical record retrieval and legal tech delivered to your inbox.