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