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Penumbra JET 7 Catheters with Xtra Flex Technology

Leading Justice is offering limited JET 7 Catheter with Xtra Flex Technology advertising and virtual secretarial services for mass tort law firms pursuing an increased case docket of Penumbra JET 7 Xtra Flex Catheter injury claims. With more than 15 years of experience helping consumers harmed by defective medical devices and the staying power of an honest, 100% fraudulent-free business history, Leading Justice has the transparency in advertising to be your partner in building a large JET 7 Xtra Flex Catheter docket. Leading Justice will create and place JET 7 Xtra Flex Catheter injury media for your buy and screen all JET 7 Xtra Flex Catheter-related contacts according to your qualifying case criteria. We will single sign the client’s claim to your retainer/medical release using the most rigorous security industry certification standards and send the signed JET 7 Xtra Flex Catheter injury claim to your intake team for the final screen and medical record retrieval.

If your firm is interested in pursuing JET 7 Xtra Flex Catheter-associated injury claims, Leading Justice can build your docket via our effective advertising and virtual secretarial services. Law firms partnered with Leading Justice know they are working with an honest, transparent advertising shop that will build their JET 7 Xtra Flex Catheter injury docket with marketing best practices and bar opinions in mind.

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JET 7 Xtra Flex Catheter Contacts

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Categories: Medical Devices, Penumbra JET 7 Xtra Flex Catheter. Tags: arterial rupture, aspiration catheter, brain bleed, catheter recall, device fracture, hemorrhage, JET 7 Xtra Flex Catheter, JET 7 Xtra Flex Catheter recall, penumbra, stroke, vessel damage, wrongful death.
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  • Description
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Product Description

Leading Justice is a full-service marketing company working with law firms on a cash-buy basis to sign up fully qualified, fraud-free JET 7 Xtra Flex Catheter-related injury cases. Here at Leading Justice, we can customize your firm’s JET 7 Xtra Flex Catheter advertising needs and help you sign up cases via internal cash buys. Our clients only pay an agency fee to cover the cost of JET 7 Xtra Flex Catheter advertising, plus a fee for each case we sign, and any data we generate for your firm belongs to you. We also cross-qualify all of our contacts, which means any data we generate that doesn’t qualify for the target campaign is evaluated to determine whether it qualifies for another type of claim. By using innovative approaches to target contacts specifically related to the JET 7 Xtra Flex Catheter and side effects like hemorrhage, vessel damage, arterial rupture and wrongful death, Leading Justice will increase your firm’s JET 7 Xtra Flex Catheter caseload. If you are interested in helping victims of JET 7 Xtra Flex Catheter side effects and complications, our direct advertising strategies and extensive consumer reach at Leading Justice gives you the competitive edge and confidence you need to allocate your full budget, knowing that your money is being spent in the best way possible.

Each law firm we work with at Leading Justice plays a critical role in determining how we categorize claims as qualified or not. And while our experience working with plaintiff law firms allows us to recognize a great case when we see one, we will tailor our JET 7 Xtra Flex Catheter intake specifications to the exact criteria you are seeking. So, if your firm has specific JET 7 Xtra Flex Catheter qualifying case criteria you want us to use, we can train our intake specialists to apply the criteria to each email and phone call they receive. By getting rid of the middle man, Leading Justice offers clients an opportunity for internal cash buys of JET 7 Xtra Flex Catheter injury data with no chance of fraud.

JET 7 Xtra Flex Catheter Litigation

Penumbra’s JET 7 Xtra Flex Catheter is an aspiration catheter commonly used during thrombectomy procedures to remove blood clots and restore blood flow in patients experiencing an acute ischemic stroke. An ischemic stroke occurs when the flow of blood through an artery in the brain is blocked by a blood clot, or a mass of thickened blood, also known as a thrombus. If left untreated, the clot can cut off the supply of blood to the brain and cause potentially life-threatening complications, such as stroke. A common treatment for the removal of dangerous blood clots in the brain is a thrombectomy. During this procedure, a catheter like Penumbra’s JET 7 Xtra Flex Catheter is inserted into the patient’s blood vessel to remove the blockage (the blood clot) and restore blood flow to the affected area. However, Penumbra has indicated that the JET 7 Xtra Flex Catheter “may become susceptible to distal tip damage during use,” which can result in “potential vessel damage, and subsequent patient injury or death.”

The FDA announced Penumbra’s urgent recall of more than 30,000 JET 7 Xtra Flex Catheters in December 2020, notifying healthcare providers that the use of the catheters during clot removal procedures is associated with an increased risk of mortality and serious injury. The recall was issued after the FDA received more than 200 medical device reports citing product malfunctions, serious injuries and patient deaths associated with the JET 7 Xtra Flex Catheter and JET 7MAX configuration, which includes the JET 7 Xtra Flex Catheter and MAX Delivery Device. According to the FDA recall notice, the distal tip of the recalled JET 7 Xtra Flex Catheters may break, fracture or expand during use, which can rupture the blood vessel while a clot is being removed from the brain and put patients at risk for serious and potentially life-threatening complications like hemorrhage, cerebral infarction (stroke) or wrongful death. Individuals who have suffered injuries or lost a loved one as a result of problems with Penumbra’s JET 7 Xtra Flex Catheter may be eligible to pursue compensation from Penumbra through a product liability lawsuit.

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