September 13, the U.S. Food and Drug Administration announced a recall on a drug infusion pump by Medtronic.

The recalled drug pump was called “SynchroMed II”, including models of 8637-20 and 8637-40, distributed between 2004 and July 2011.

There is a problem that actually causes recurrent or withdrawal symptoms, which could be life-threatening.  There are 55 known cases of failure, and one known death.  I personally might know of another unreported death, someone who died just two months after having a pain pump put in. It was a painfully slow death because her own doctors didn’t know what was going on.  She was a single mom.