Archive | June, 2010

Mylotarg (gemtuzumab ozogamicin): Market Withdrawal

21. June 2010

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Drug failed to demonstrate clinical benefit to patients enrolled in trials.

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Magic Power Coffee: Undeclared Drug Ingredient

21. June 2010

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Product marketed as a dietary supplement for sexual enhancement contains the drug ingredient hydroxythiohomosildenafil, a chemical that may interact with prescription nitrates, and cause dangerously low blood pressure.

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Tamiflu: Counterfeit Product Sold on Internet

17. June 2010

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Potentially harmful product represented as “Generic Tamiflu”- tests revealed product does not contain oseltamivir, but cloxacillin, an antibiotic.

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Vitamin D Supplement Products: Medication Use Error

15. June 2010

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Some liquid Vitamin D supplement products are sold with droppers that could allow parents to accidentally give harmful amounts of Vitamin D to their infant.

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Hospira Brand Liposyn and Propofol: Recall

10. June 2010

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Injectable products may contain particulate matter.

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Defibtech DBP-2800 Battery Packs used in Lifeline AED and ReviveR AED: Recall

9. June 2010

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AED may falsely detect an error condition during charging for a shock, then cancel charge and not provide therapy, when used with an affected battery pack.

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Counterfeit Polypropylene Surgical Mesh: Initial Communication

8. June 2010

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[UPDATED 06/08/2010] Recall classified as Class I. Various sizes of counterfeit flat sheets of polypropylene surgical mesh marketed in the U.S. labeled with the C. R. Bard/Davol brand name.

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GammaGard Liquid, Immune Globulin Intravenous (Human)

4. June 2010

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Market withdrawal due to an increased number of adverse event reports of allergic reactions associated with two lots.

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