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March 24, 2026
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Mar

FDA Recall: Software error could result in inaccurate insulin delivery.

March 24, 2026
Company: Medtronic MiniMed, Inc Date of Enforcement Report: 3/24/2026 Class: II PRODUCT: MiniMed” 780G – MMT-1884 MiniMed” 780G – MMT-1886 With Software 6.60 and 6.61 Recall Number: Z-1635-2026 REASON: Three software defects (Pump Error 53, BG check, and Critical Pump Error (Open Book Image)) that occurred as a result of software updates (versions 6.60, 6.61,...
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