WebYour medical provider used a Penumbra JET 7 Xtra Flex catheter in the procedure to remove the clot. The use of the Penumbra JET 7 catheter during the procedure caused an injury … WebFor a FREE, no-obligation consultation with an experienced Penumbra lawsuit lawyer, please call 1-800-525-7111 or complete the convenient form below. There is no obligation and …
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WebPenumbra JET 7 Catheter Injury Lawyers Penumbra’s Urgent Voluntary Recall of JET 7 Catheters with Xtra Flex Technology The U.S. Food and Drug Administration (FDA) has received more than 200 reports about the Penumbra JET 7 Reperfusion Catheter with Xtra Flex Technology, which has been used in stroke patients to remove blood clots. Web9. mar 2024 · The Penumbra JET 7 Catheter and FDA Approval. Along with a pump and tubing, this catheter is part of Penumbra’s mechanical thrombectomy set. This process uses a vacuum pump to clear blood clots. The JET 7 also uses low levels of radiation to detect severe clots. Penumbra claims that this procedure can remove blood clots from stroke … bomb levels clash of clans
Penumbra JET 7 Catheters Lawyers · Pharmaceutical Litigation
Web15. jan 2024 · The Penumbra catheter defects reportedly cause the device’s tip to balloon, expand, rupture, break, completely separate, or even expose internal support coils. These defects can lead to patient injuries such as vessel damage, hemorrhaging, and continued blockage of blood vessels. In some situations, these complications can be deadly. WebThe Penumbra Jet 7 Xtra Flex Catheter is a medical device that allows doctors to remove blood clots in stroke patients and restore blood flow. Doctors use the catheter in patients who don’t respond to clot-busting drugs. Penumbra issued a recall in December 2024 after reports of serious injury and death. WebPenumbra warned healthcare providers that the catheter’s distal tip could cause damage to vessels along with other injuries, including death. Penumbra eventually issued an urgent voluntary recall on December 15, 2024 for all Jet 7 Xtra Flex Catheter units following the more than 200 reports submitted to the FDA. bombled paris