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HSMN NewsFeed - 11 Mar 2009
FDA Classifies Recent Urgent Device Correction on Baxter's COLLEAGUE Infusion Pump as a Class I Recall
FDA Classifies Recent Urgent Device Correction on Baxter's COLLEAGUE Infusion Pump as a Class I Recall
HSMN NewsFeed - 25 Jul 2007
FDA Classifies Baxter's Voluntary Recall Action Regarding Service Documentation as a Class I Recall
FDA Classifies Baxter's Voluntary Recall Action Regarding Service Documentation as a Class I Recall
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Volumetric Infusion Pump
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Volumetric Infusion Pump
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