6 results

• Penumbra Catheter Recall Over JET 7 Xtra Flex Tip Damage Categorized as Class I by FDA

  February 1, 2021

  Irvin Jackson

  The FDA has issued a Class I classification to a Penumbra Jet 7 Xtra Flex Catheter recall, following reports of deaths and severe patient injuries.

• Deadline Established For Lead Plaintiff in Class Action Lawsuit Over Penumbra Jet 7 Xtra Flex Catheter

  January 28, 2021

  Irvin Jackson

  Investors seeking to participate in a recently filed Penumbra Jet 7 Xtra Flex catheter class action lawsuit have until March 16 to file a complaint if they want to be a lead plaintiff in the litigation.

• Penumbra Catheter Problems Results in Class Action Lawsuit After Jet 7 Xtra Flex Recall

  January 19, 2021

  Irvin Jackson

  A class action lawsuit accuses of Penumbra of misleading investors by not telling them of problems with its Jet 7 Xtra Flex catheters, which eventually led to a recall and a significant drop in the company's stock market value.

• Penumbra Jet 7 Catheters Carry Risk of Serious Injury and Death, FDA Warns

  December 17, 2020

  Martha Garcia

  The FDA is urgently informing health care personnel of a JET 7 Xtra Flex catheter recall following two hundred incident reports and 14 deaths due to device failures.

• Penumbra Brain Catheter Recall Issued Due to Manufacturing Error

  December 9, 2010

  Staff Writers

  A recall has been announced for the Penumbra System Reperfusion Catheter 32 due to a manufacturing error, which could cause...

• Penumbra Catheter Recall Issued for Neuron 6F 070 Delivery Catheter

  October 2, 2009

  AboutLawsuits

  Older versions of Penumbra Inc.’s Neuron 6F 070 Delivery Catheter have been recalled in the wake of reports that some...