Bayer announces voluntary recall on additional lots of Kogenate FS Antihemophilic Factor (Recombinant).
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Medical Advisories
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Thursday, August 11, 2016 CSL Behring extends voluntary recall of two lots of Helixate FS with vial adapter . |
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Monday, July 25, 2016 CSL Behring has announced a recall of 2 lots of Helixate FS due to loss of potency. |
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Monday, July 25, 2016 Bayer announces a recall of 2 lots of Kogenate FS due to loss of potency. |
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Friday, July 8, 2016 Kedrion Biopharma is placing a voluntary, temporary hold on future shipments of Koate DVI. |
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NHF’s Medical and Scientific Advisory Council (MASAC) has assessed three recent publications suggesting elevated inhibitor rates in a specific product. |
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Covidien, a healthcare products company, initiated a voluntary recall of certain lots of MonojectTM prefill flush syringes due to the syringes being filled with water that had not been subjected to their autoclave sterilization process. |
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Wednesday, October 26, 2011 In January 2011, NHF issued a Medical Advisory (#412) about a recall of nonsterile alcohol wipes produced by one company, Triad Group, Inc. |
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Wednesday, November 16, 2011 Baxter Healthcare Corporation has sent a notice of a labeling error affecting the expiration date of the Sterile Water for Injection that is packaged as a diluent with Recombinate [Antihemophilic Factor (Recombinant)]. |
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Thursday, July 28, 2011 Baxter BioScience has announced that it is voluntarily recalling one lot of Recombinate Antihemophilic Factor (Recombinant). Baxter states that this recall is being taken as a precautionary measure after a retrospective review of its manufacturing process revealed a breach in aseptic processing. |