Maude Monthly: Abbott CGM Low Reading Problem Continues to Grow as Company Discloses Additional Death; Medline Reports Hundreds of Late Reports in Wake of FDA Scrutiny; MAUDE Data Reveals Additional Issue with Insulet Omnipod

The information contained in this report is compiled from the FDA’s Manufacturer and User Facility Device Experience (MAUDE) database. The MAUDE database contains reports of deaths, injuries, and malfunctions relating to the use of medical devices and is updated monthly with reports from users, physicians, and device manufacturers. The FDA uses MAUDE reports to monitor […]

Published on Jul 15, 2026

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