This insulin pump has been recalled over flaw that’s killed 1 and injured nearly 2,200
The FDA announced an international Class 1 recall of 322,005 Medtronic’s MiniMed 600 Series Insulin Pumps that can cause the user to receive an incorrect amount of insulin.
According to the recall notice, Medtronic has heard 26,421 complaints, 2,175 injuries and one death. That’s why the FDA makes this a Class 1 recall, which means, “use of these devices may cause serious injuries or death.”
What’s covered in this insulin pump recall?
All lots of MiniMed Model 630G from before October 2019 and all lots of MiniMed Model 670G from before August 2019. Medtronic began notifying customers of a possible problem on Nov. 21.
The retainer ring problem
The pumps might have a missing or broken retainer ring. The retainer ring helps lock the insulin cartridge into place in the pump’s reservoir compartment.
“If the cartridge is not locked firmly into place, under or over delivery of insulin may occur, which could result in hypoclycemia or hyperglycemia. Severe hyperglycemia can result in a loss of consciousness, seizure, and death.”
What customers should do
Check the retainer ring. If it’s loose, damaged or just not there, contact Medtronic at 877-585-0166 and stop using the pump. Check with your doctor for guidance. Do manual injections.
This story was originally published February 12, 2020 at 11:22 AM.
