In the past few days, you may have heard that the FDA issued a Class I Recall of Medtronic SynchroMed II, SynchroMed EL Implantable Infusion Pump and Refill Kits. Although Class I is the most serious level of recall, used for a situation in which there is a reasonable probability that the use o...


Thank you so much for your insight on this issue. I have one of the pumps "recalled" and found about this ONLY from Chronic Pain, not my doctor, which is upsetting. Sometimes I don't know what I would do without Chronic Pain.
I also have a recalled pain pump.
My pump doctor did NOT know what I was talking about.
Thanks To Health Central now I know whats going on with my pain pump.
THANK YOU and KEEP UP THE GREAT WORK THAT YOU ARE ALL DOING.