Medtronic Receives FDA Warning Letter for Insulin Pump Recall
The warning letter from the FDA is related to recalls of the MiniMed 600 series insulin infusion pump, and a device for MiniMed 508 and Paradigm pumps.
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Search Results for: diabetes
FDA Grants Breakthrough Designation for Noninvasive Glucose Monitoring Technology
The FDA recognized a non-invasive continuous glucose monitoring system that measures glucose levels in the blood via radiofrequency waves.
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Home Medical Equipment Market Expected to Reach $56 Billion by 2027
The size of the global home medical equipment market is estimated to reach $56 billion by 2027, according to a report from Allied Market Research.
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Device Used by Many Diabetics at Center of Wrongful Death Lawsuit in Georgia
An Atlanta resident died of hypoglycemia after his Dexcom G6 glucose monitoring device failed to sound an alarm; his widow is pursuing a wrongful death suit.
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Medtronic Insulin Pump Devices Recalled Due to Serious Risks
The U.S. FDA has issued a Class I recall on Medtronic’s wireless insulin pump remote controllers. The FDA notified patients of the recall—the most serious type—because of problems with the devices that could cause serious injury or death.
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