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Home » Two Medtronic Pumps Recalled
Two Medtronic Pumps Recalled
February 1, 2013
Medtronic is advising customers not to use unapproved drugs with SynchroMed infusion pumps distributed between April 1999 and November 2012, due to a heightened rate of adverse events. Drugs not designated specifically for use with the SynchroMed II and SynchroMed EL implantable pumps can lead to a 7 percent failure rate after 78 months, the voluntary Class I recall notice states. The failures may cause the pumps’ motor to temporarily or permanently stall, interrupting infusion.
The GMP Letter
The GMP Letter
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