The FDA has issued a recall for a popular insulin pump used by thousands of patients with Type 1 diabetes.
The recall applies to certain Medtronic Mini-med 600 series Insulin pumps.
According to the FDA, one patient has died and more than 2,000 have been injured by the devices.
The faulty pumps deliver incorrect insulin dosing which leads to serious medical complications. The defect has to do with a retainer ring that does not properly lock in the insulin cartridges.
The recall includes about 322,000 devices.
The FDA says they have received more than 26,000 complaints about the Medtronic Insulin Pumps.
Diabetic patients with the devices are encouraged to call Medtronic or talk to their doctor or pharmacist.
If their device is defective, the company will replace it. but they will need to use insulin injections in the interim.
For more details on the recall visit