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FDA Drug & Medical Device Recall News & Comments 
Wednesday, September 09 2009

Penumbra Neuron 5F Select Catheter Recall

Penumbra and FDA notified healthcare professionals of the Class 1 recall of the Neuron 5F Select Catheter, used to remove blood clots or foreign objects from blood vessels. Due to a manufacturing error, the catheters may contain pin holes and exposed wire braids which may result in a brain clot or a blood vessel puncture, and this may lead to possible death. The device was distributed from May 5, 2009 through June 12, 2009.

Any adverse events or quality problems that may be related to the use of this product should be reported to the FDA's MedWatch Adverse Event Reporting program online, by phone [1-800-332-1088], or by returning the postage-paid FDA Form 3500 by mail [to MedWatch, 5600 Fishers Lane, Rockville, MD 20852-9787] or fax [1-800-FDA-0178].

SEE: Catheter Recall - Penumbra Neuron 5F Select Catheter Recall and Penumbra 6F Neuron 070 Delivery Catheter Recall - Stroke & Death Lawsuits

Penumbra Neuron 5F Select Catheter Lawsuit - Talk to a Lawyer

If you or a loved one have suffered a serious injury, stroke or heart attack or you have lost a loved one, as a result of the use of a Penumbra Catheter, then please call us for a Free Confidential Case Consultation. Talk to a Board Certified Personal Injury Trial Lawyer with more than 25+ years of experience call 1-800-883-9858

Posted by: dw AT 05:29 pm   |  Permalink   |  Email
Willis Law Firm - Houston, Texas Drug Injury Lawyer and Attorney Free Lawsuit & Class Action Lawsuit Lawyer

 

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