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  2. St. Jude to Face Products Claim Over Allegedly Faulty Medical ...

    www.aol.com/news/st-jude-face-products-claim...

    The ruling, from U.S. Magistrate Judge Christopher J. Burke, jettisoned claims by Kathleen M. Freed that St. Jude had failed to live up public guarantees regarding the safety of its spinal cord ...

  3. Telectronics - Wikipedia

    en.wikipedia.org/wiki/Telectronics

    The cause of the recall was a "J lead" electrode, utilizing a rigid stylet within the helix of the electrode lead, inherited by the company in acquisition of pacemaker lead manufacturer Cordis Corporation of Miami. The inherent dangers arising from incorporation of a rigid stylet had been demonstrated by Telectronics, Sydney, in 1967.

  4. St. Jude Medical Signs Equity Investment and Option to ... - AOL

    www.aol.com/news/2013-06-07-st-jude-medical...

    St. Jude Medical Signs Equity Investment and Option to Purchase Agreement with Spinal Modulation Agreement provides St. Jude Medical immediate international distribution rights for the Axium ...

  5. St. Jude Medical - Wikipedia

    en.wikipedia.org/wiki/St._Jude_Medical

    St. Jude Medical was founded in 1976 to further develop bi-leaflet artificial heart valves, which were originally created in 1972 at the University of Minnesota. [4] [5] St. Jude Medical's bi-leaflet valve was developed in large part by Dr. Demetre Nicoloff of the University of Minnesota and St. Jude Medical employee Don Hanson.

  6. St. Jude Invests in Spinal Cord Stimulation for Pain ... - AOL

    www.aol.com/news/2013-06-09-st-jude-invests-in...

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  7. Spinal cord stimulator - Wikipedia

    en.wikipedia.org/wiki/Spinal_cord_stimulator

    A spinal cord stimulator (SCS) or dorsal column stimulator (DCS) is a type of implantable neuromodulation device (sometimes called a "pain pacemaker") that is used to send electrical signals to select areas of the spinal cord (dorsal columns) for the treatment of certain pain conditions.

  8. FDA recall policies - Wikipedia

    en.wikipedia.org/wiki/FDA_recall_policies

    FDA's role under the guidelines is to monitor company recalls and assess the adequacy of a firm's action. After a recall is completed, FDA makes sure that the product is destroyed or suitably reconditioned and investigates why the product was defective. Generally, FDA accepts reports and other necessary recall information submitted by e-mail.

  9. FDA: Recall of St. Jude Heart Surgery Device Is Most ... - AOL

    www.aol.com/news/2013-02-14-fda-recall-of-st...

    The Food and Drug Administration has announced on its website that medical device maker St. Jude Medical last month recalled a device used in heart surgery because of the risk that it could cause ...