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