The FDA has classified the JET 7 Reperfusion Catheters Recall as a Class 1-recall, which is the most serious.
If you’ve been seriously injured by a JET 7 Reperfusion Catheters with Xtra Flex Technology by Penumbra in South Carolina, then call us at 864-235-4999 by tapping the button below or by filling out our request form for a free consultation.
For almost 20 years, I have represented numerous clients in cases involving medical malpractice and personal injury. We are here for you and will be by your side even after there’s a resolution in your case.
Information on the JET 7 Reperfusion Catheters Recall
The JET 7 Reperfusion Catheters recall was issued by Penumbra (the manufacturer) due to an increased risk of mortality and serious injury. The catheter is used to remove clots from acute stroke patients. According to a report on the FDA’s website, all users should stop using the following catheter models:
- Jet 7 Xtra Flex catheter
- JET 7MAX configuration (which includes the JET 7 Xtra Flex catheter and MAX Delivery Device
The recall does not apply to the Penumbra JET 7 Reperfusion Catheter with Standard Tip.
According to an FDA MedWatch report, “The FDA has received over 200 medical device reports associated with the JET 7 Xtra Flex catheter, including death, serious injuries, and malfunctions.” You can learn more about the recall by clicking the button below.
Did a South Carolina doctor or other South Carolina health care provider use a JET 7 and caused you injury? Call us and we can discuss a potential case. There have been 200 reports submitted to the FDA involving death, serious injuries and malfunctions.
If you have been injured by a JET 7 Extra Flex Catheter in South Carolina, please don’t hesitate to contact us today through the contact form below or by calling us at 864-235-4999.
[contact-form-7 id=”3838″ title=”Contact Us”]