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Medtronic Recalls MiniMed Insulin – Risk of Diabetic Coma

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Medtronic recently recalled more than 322,000 MiniMed insulin pumps with broken or missing retainer rings that led to at least one death, thousands of injuries, and numerous lawsuits. The recall arose after broken or missing retainer rings were observed on the devices. The ring defect that could prevent the insulin cartridge from being locked into place and, as a result, cause people to receive too much or too little insulin.

Insulin overdose can lead to hypoglycemia, a condition in which the blood sugar is lower than normal, leading to lethargy and insulin shock. Underdosage may cause hyperglycemia, which occurs when there are high levels of sugar (glucose) in the blood. Hyperglycemia can lead to a severe condition known as diabetic ketoacidosis (DKA). Without treatment, someone with DKA is in danger of falling into a diabetic coma.

MiniMed Recall Most Serious for Medical Devices

The Class I recall (the most serious type for medical devices) affects all lots of the Model 630G (MMT-1715) manufactured before October 2019 and all lots of Model 670G (MMT-1780) manufactured before August 2019. If you own a MiniMed insulin pump that is part of the recall, you should take the following action:

If the reservoir locks properly, Medtronic advises that you continue to use the pump. If the pump is dropped or damaged accidently, you should check the ring for damage.

According to the FDA, there have been over 26,000 complaints concerning the MiniMed insulin pump. However, despite the fact that the device might cause serious injury or death, it remains approved for use in the U.S.

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