(HealthDay)—More than 322,000 MiniMed 600 Series Insulin Pumps have been recalled by Medtronic due to a defect that could cause them to malfunction and put users at risk for serious harm or death.
The recalled devices lack or have a broken retainer ring that helps lock the insulin cartridge into place in the pump’s reservoir compartment. If the cartridge is not locked firmly into place, too little or too much insulin may be delivered, which could result in hypoglycemia or hyperglycemia, the U.S. Food and Drug Administration said.
Medtronic has received 26,421 complaints about malfunctions in the recalled insulin pumps and is aware of 2,175 injuries and one death. The Class I recall—the most serious type—is for Model 630G (MMT-1715), including all lots before October 2019, and for Model 670G (MMT-1780), including all lots before August 2019.
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