Home » 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
KEYWORDS FDAnews Device Daily Bulletin
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