On October 6, 2008 my son (15 years old, type 1 diabetic) showed flu like symptoms, his pump was showing normal delivery of meds, etc. By the next morning he was rushed to the hospital and almost died. He spent several hours in the emergency room and was then transported to another hospital and stayed 3 days in intensive care. No one could determine what the problem was but it appeared he didn’t get any insulin for 32 hours. The only explanation that was given was that perhaps the infusion set hit some muscle. On and I reported this to Medtronic. When the recall happened I found that all the infusion sets we’ve received for my son for the last 1 1/2 years have been lot 8. I called Medtronic again to document the case and wondered if anyone has a suggestion on where to go from here. I’m sure that the problem experienced with my son in October was related to the Lot 8 infusion sets.