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www.fdanews.com/articles/62004-mhra-issues-alert-on-baxter-infusion-pump

MHRA ISSUES ALERT ON BAXTER INFUSION PUMP

August 24, 2006

The Medicines & Healthcare products Regulatory Agency (MHRA) in the UK has issued a medical device alert for Baxter Intermate and Infusor large volume (LV) infusions pumps because of an increased risk that the device's elastomeric balloon may burst during infusion.
MHRA