Penumbra Catheter Recall Over JET 7 Xtra Flex Tip Damage Categorized as Class I by FDA
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.
Tag Archives: Penumbra Catheter
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Deadline Established For Lead Plaintiff in Class Action Lawsuit Over Penumbra Jet 7 Xtra Flex Catheter
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…
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Penumbra Catheter Problems Results in Class Action Lawsuit After Jet 7 Xtra Flex Recall
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…
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Penumbra Jet 7 Catheters Carry Risk of Serious Injury and Death, FDA Warns
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.
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Penumbra Brain Catheter Recall Issued Due to Manufacturing Error
A recall has been announced for the Penumbra System Reperfusion Catheter 32 due to a manufacturing error, which could cause the devices to fail and lead to life-threatening injury.
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Penumbra Catheter Recall Issued for Neuron 6F 070 Delivery Catheter
Older versions of Penumbra Inc.’s Neuron 6F 070 Delivery Catheter have been recalled in the wake of reports that some catheters have kinked, ovalized or broken, resulting in injuries.
