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Trustwell Law is accepting Bard PowerPort cases nationwide on behalf of people who had a PowerPort device and suffered from one or more of these injuries and issues:
If you or a loved one had a Bard PowerPort implanted, experienced any of these injuries, and are considering filing a Bard PowerPort lawsuit, call us at 800-796-1636 or submit your case details online and someone will contact you shortly. You pay nothing unless your lawsuit is successful and you receive compensation.
At Trustwell Law, our experienced attorneys take a personalized, compassionate approach. We cut through the legalese and partner with our clients. We also have access to the expertise, resources, and manpower to fully investigate each case and fight for and with our clients to get the justice they deserve.
The Bard PowerPort is a group of implantable port devices, inserted below the skin, to connect to a catheter to deliver medicine and fluids to the bloodstream. Port catheters allow simple access to a patient’s veins. They are used for patients who need regular treatments with medications, such as chemotherapy.
The port contains a small reservoir into which medicine is injected. A doctor implants the device under the skin. The catheter rests inside the vein.
As patients receive medication through the Bard PowerPort, the design causes the injection flow to increase, which creates pressure against the plastic tubing. People filing Bard PowerPort lawsuits claim this design flaw increases the risks of organ damage, infection, and blood clots. The catheter can break, move, or crack under the pressure.
Allegations against Becton Dickinson, the medical technology company that manufactures and sells the Bard PowerPort, claim it concealed thousands of reports from doctors and patients citing injuries caused by the device. This means the company may have known about the device’s flaws and issues for years before the FDA issued its recall.
If you or a loved one suffered any of the injuries listed above after having the Bard PowerPort device implanted or if a loved one died after using the device, contact us to discuss filing a Bard PowerPort lawsuit. The consultation is free. You pay nothing unless you win your case and receive compensation.
Sources
BD.com. (n.d.). PowerPort Implantable Port. Retrieved from https://www.bd.com/en-us/products-and-solutions/products/product-page.1759601#overview
Brittain, B. (2023, February 17). Bard convinces U.S. appeals court to revive medical-injection device patents. Retrieved from https://www.reuters.com/legal/bard-convinces-us-appeals-court-revive-medical-injection-device-patents-2023-02-17/
Bronstad. A. (2023, July 3). ‘Shockingly Large Number of People’ Could Sue Over Bard’s PowerPort Device. Retrieved from https://www.law.com/2023/07/03/shocking-large-number-of-people-could-sue-over-bards-powerport-device/
FDA. (2020, March 26). Class 2 Device Recall Power Port Implantable Port. Retrieved from https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRES/res.cfm?start_search=1&event_id=84914
Health Sciences Authority. (2019, September). Attention: Risk Manager/Materials Manager. Urgent Medical Device Recall Notification. Implantable Ports & Groshong Central Venous Catheter. Retrieved from https://www.hsa.gov.sg/docs/default-source/announcements/field-safety-notices/hsa-6004101-050-19-04_64-fsn.pdf
Heng, T.H. et al. (2022, September 1). Infection of a venous port – beware of the Mycobacterium. Retrieved from https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9584557/
Pike, S., K. Tan, and B. Burbridge. (2021, December 15). Complications Associated With Totally Implanted Venous Access Devices in the Arm Versus the Chest: A Short-Term Retrospective Study. Retrieved from https://journals.sagepub.com/doi/abs/10.1177/08465371211040822
Wu, C. et al. (2021, October 27). Does catheter material affect functional performance of intravenous ports via the superior vena cava? Retrieved from https://journals.plos.org/plosone/article?id=10.1371/journal.pone.0253818
You will never be charged a fee unless a recovery is made for you.