Manufacturer
38 recalls in our database name Medtronic MiniMed, Inc. as the manufacturing or recalling firm.
The manufacturer string comes from the agency’s own source notice — for FDA recalls, the “recalling firm” field; for NHTSA recalls, the vehicle manufacturer; for CPSC recalls, the firm-of-record on the joint press release. A single corporate family can appear under multiple manufacturer strings as agency notices aren’t standardized on a canonical name. If you don’t see recalls you expect, try a parent-company search or a broader full-text search.
Severity scores below are computed from the agency’s classification and the recall text, never from manufacturer behaviour or history. Many manufacturers issue routine corrective actions (software updates, labelling corrections) that are correctly scored low — having recalls on this list isn’t inherently a quality signal.
Medtronic MiniMed's 780G Insulin Pump can stop delivering insulin due to a software anomaly when paired with the Instinct sensor, potentially leading to delayed therapy and increased risk of hyperglycemia or diabetic ketoacidosis.
Pending LLM rewrite. Source: FDA_DEVICE Z-1743-2026.
Pending LLM rewrite. Source: FDA_DEVICE Z-1748-2026.
Pending LLM rewrite. Source: FDA_DEVICE Z-1741-2026.
Pending LLM rewrite. Source: FDA_DEVICE Z-1751-2026.
Pending LLM rewrite. Source: FDA_DEVICE Z-1752-2026.
Pending LLM rewrite. Source: FDA_DEVICE Z-1750-2026.
Pending LLM rewrite. Source: FDA_DEVICE Z-1740-2026.
Pending LLM rewrite. Source: FDA_DEVICE Z-1744-2026.
Pending LLM rewrite. Source: FDA_DEVICE Z-1745-2026.
Pending LLM rewrite. Source: FDA_DEVICE Z-1749-2026.
Pending LLM rewrite. Source: FDA_DEVICE Z-1742-2026.
Pending LLM rewrite. Source: FDA_DEVICE Z-1739-2026.
Pending LLM rewrite. Source: FDA_DEVICE Z-1747-2026.
Pending LLM rewrite. Source: FDA_DEVICE Z-1746-2026.
Pending LLM rewrite. Source: FDA_DEVICE Z-1635-2026.
Pending LLM rewrite. Source: FDA_DEVICE Z-1238-2026.
Pending LLM rewrite. Source: FDA_DEVICE Z-0958-2026.
Pending LLM rewrite. Source: FDA_DEVICE Z-0594-2026.
Pending LLM rewrite. Source: FDA_DEVICE Z-0033-2026.
Pending LLM rewrite. Source: FDA_DEVICE Z-2496-2025.
Medtronic MiniMed is recalling InPen smart insulin pens that may have been incorrectly assembled, potentially causing the insulin cartridge to not fit or the cartridge holder to be difficult to remove. Users without backup insulin could experience temporary hyperglycemia.
Medtronic MiniMed's Paradigm insulin pumps can malfunction during airplane flight due to air pressure changes, potentially causing dangerously high or low blood sugar levels that could be fatal.
Medtronic MiniMed 720G insulin pumps may malfunction during airplane travel due to air pressure changes, causing abnormal insulin doses that can lead to severe low or high blood sugar emergencies.
Medtronic MiniMed insulin pumps may deliver abnormal insulin doses during airplane takeoff or landing due to air pressure changes, potentially causing severe low or high blood sugar.