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

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

    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 ...

  3. 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.

  4. Drug recall - Wikipedia

    en.wikipedia.org/wiki/Drug_recall

    A drug recall removes a prescription or over-the-counter drug from the market. Drug recalls in the United States are made by the FDA or the creators of the drug when certain criteria are met. When a drug recall is made, the drug is removed from the market and potential legal action can be taken depending on the severity of the drug recall. [1]

  5. 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.

  6. FDA issued over 20 recalls in August. Check this list to see ...

    www.aol.com/fda-issued-over-20-recalls-182642974...

    The FDA has announced over 20 recalls across the U.S., including food items, cosmetics, drugs, dietary supplements, and medical devices.

  7. Another Heartache for St. Jude - AOL

    www.aol.com/news/2013-02-14-another-heartache...

    The hits keep on coming for St. Jude Medical . Fresh off earnings that showed the continued decline of its cardiac rhythm management, or CRM, sales, St. Jude took a fresh cardio kick this week ...

  8. Medical device reporting - Wikipedia

    en.wikipedia.org/wiki/Medical_device_reporting

    Medical device reporting (MDR) is the procedure for the Food and Drug Administration to get significant medical device adverse events information from manufacturers, importers and user facilities, so these issues can be detected and corrected quickly, and the same lot of that product may be recalled.

  9. Why St. Jude Medical Shares Were Zapped - AOL

    www.aol.com/2012/11/21/why-st-jude-medical...

    What: Shares of medical device maker St. Jude. Although we don't believe in timing the market or panicking over market movements, we do like to keep an eye on big changes -- just in case they're ...

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