Recall of Medtronic MiniMed 720G Insulin Pump
Areazine synthesizes this FDA recall directly from FDA's official public data feed. See our methodology for full source attribution and refresh cadence.
Medtronic MiniMed, Inc. is recalling 37,458 units of the MiniMed 720G Insulin Pump due to potential unintended over- or under-delivery of insulin caused by gravitational forces, which could lead to severe health risks.
What this FDA recall tells you, and what most readers miss
This notice was issued by FDA on April 14, 2026 and geographically references United States. Its severity classification of "high" signals how the issuing agency weighs the risk of harm if no action is taken - "critical" and "high" tier alerts typically carry direct consumer actions, while "medium" and "low" tend toward informational guidance or monitoring advisories. The category it belongs to - FDA Recalls - determines the consumer-protection framework behind it, which shapes what remedies (refunds, replacements, repairs, or the recall itself) are available to affected consumers and which agency holds statutory responsibility for enforcement.
Most readers skim a notice like this, check whether they are personally affected, and move on. The more useful lens is to verify its scope, source, and timestamp, then compare related notices without assuming that one record proves a broader trend.
Areazine pairs this record with the original agency URL so you can check the primary source before acting. Its related labels are recall, product-safety, fda, Devices.
What Happened
Medtronic MiniMed, Inc. is recalling its MiniMed 720G Insulin Pumps because they may cause unintended over- or under-delivery of insulin due to changes in gravitational force, potentially leading to severe hypoglycemia, seizure, coma, death, severe hyperglycemia, dehydration, diabetic ketoacidosis, or death.
Which Products Are Affected
The affected products are the MiniMed 720G Insulin Pump with model numbers MMT-1809, MMT-1810, MMT-1859, MMT-1860, and MMT-1867. The recall involves 37,458 units distributed worldwide, including US nationwide in states such as OR, CA, AZ, NY, TX, FL, OH, MO, TN, NJ, NC, SC, IL, VA, WA, DC, GA, PA, MS, IA, MI, NH, OK, SD, MT, WI, WV, MA, LA, MN, RI, AR, ME, AL, IN, UT, KY, CO, ND, MD, CT, NM, KS, ID, NV, DE, NE, VT, AK, HI, WY, PR, and VI, as well as various international countries. The recall number is Z-1745-2026, and related UDI-DI codes include 763000854768, 763000505196, among others listed in the code info.
What You Should Do
Consumers who have the affected MiniMed 720G Insulin Pumps should follow the initial firm notification, which was issued via letter, and contact Medtronic MiniMed, Inc. for further instructions on the recall.
Why This Matters
This recall affects a significant number of insulin pumps used by individuals with diabetes, potentially exposing them to serious health risks including severe hypoglycemia or hyperglycemia, which could result in life-threatening conditions.
Source
FDA recall notice for event ID 98186, recall number Z-1745-2026. For more information, visit the FDA website.
Original source: FDA Official Notice ↗
Related FDA Recalls
All FDA Recalls →Nationwide notices with similar length or severity timing 8
Two Areazine-derived peer sets for this FDA recall: nearest notices by body length and by same severity near the same agency date. Peers come from other categories so they are not the same-feed Related list above.
Similar body length
Nearest notices by article body length (1,594 characters here).
Similar severity timing
Same severity (high) notices issued closest in time to April 14, 2026.
Frequently Asked Questions
Common questions about this FDA recall.