Media outlets have recently reported on dozens of deaths that are believed to have resulted from malfunctioning Penumbra Jet 7 Xtra Flex Catheters. Many others have been made aware by Penumbra Catheter recall TV commercials.

  • The FDA has issued a recall on the Penumbra JET 7 Xtra Flex catheter
  • Victims of injury and their family members can seek justice and compensation
  • The Product Lawyers are ready to help you make things right

Families who have been left suffering as a result of malfunction Penumbra catheters are right to ask questions. Our experienced attorneys can help provide the answers.

Free Penumbra Recall Evaluation

(877) 671-6480

Families who have been affected by defective surgical tools deserve answers, support, and justice. Our attorneys are proud to represent these families.

— Laurence Banville, Esq.

Penumbra Catheter TV Commercials Warn Of Device Recall

Penumbra catheters have been in use for more than a decade. However, the product’s life has seen it go through many continuously-evolving iterations.

One of the most recent models, the JET 7 Xtra Flex Catheter and JET 7MAX configuration, have generated more than 200 medical device reports. In these, practitioners have described how malfunctions of the device have been involved in:

  • Device distal tip damages
  • Ballooning expansion breakages
  • Complete separation of the device while in-use

The delicate nature of the catheter’s application can entail that any malfunction, no matter how minimal, can result in serious injury. In the case of the Penumbra catheter, lawsuit TV commercials have highlighted how patients have lost their lives as a result of such defects.

If you or a loved one were the victims of a recalled Penumbra catheter, our attorneys believe you have ground for a lawsuit against the manufacturer. Learn more about your and your family’s avenues for financial compensation by contacting us today.

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Free Penumbra Catheter Lawsuit Consultations

(877) 671-6480

TV Commercials: Lawsuits Against Penumbra For Catheter Defects

Medical device manufacturers spend countless amounts of money and time developing new products. Indeed, it can cost tens of millions of dollars and years of testing before a new device can come to market.

With the substantial amount of resources devoted to a single vertical, the manufacturer can feel tremendous pressure to succeed. Often, a product making it to market can make the difference between bankruptcy and increased funding.

This need can drive companies to release dangerous devices, ones that have not undergone enough testing or improvements, pontetially placing the lives of customers at risk. At the end of the day, there is no excuse that can account for knowingly causing an unsuspecting person harm. This is even more true when the victim is a patient counting on the device to help them regain their health in one aspect or another.

As of early 2021, the FDA has already issued a recall on specific Penumbra catheter models. It is unclear whether previous Penumbra catheter models are susceptible to similar malfunctions.

Contact The Product Lawyers For A Free Penumbra Catheter Lawsuit Consultation

Did you or a family member suffer severe injuries as a result of a malfunction Penumbra catheter? You deserve justice and compensation that helps you recover.

Nothing can undo the harm that has been, but your family and you deserve to be compensated for the pain you’ve endured. Our experienced defective medical device lawyers are prepared to help you fight for full compensation.

Contact us today to get started on the path to justice.

Contact The Product Lawyers for a free consultation

(877) 671-6480