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The FDA has recalled Medtronic's (MDT) SynchroMed infusion pump following the death of 14...

The FDA has recalled Medtronic's (MDT) SynchroMed infusion pump following the death of 14 patients since 1996 due to flaws in the device. Eleven patients died because of the inadvertent injection of a drug into subcutaneous tissue rather than into the pump, while two died from a blockage and another because of an electrical short.
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  • ch61
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    27 Jun 2013, 08:02 AM Reply Like
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