Recall Z-2982-2026— Medtronic MiniMed, Inc.

Name: FDA recall Z-2982-2026
Creator: U.S. Food and Drug Administration
Published: 2026-07-13

Class II · Ongoing

Class II FDA medical device recall by Medtronic MiniMed, Inc., initiated 2026-07-13. It names one FDA 510(k) clearance: K251032. Product: MiniMed 780G Insulin Pump, Model: MMT-1885CLW, MMT-1886CLW. Reason: Loaner insulin pumps may have been cleaned with chemically incompatible products that could damage the pump case or keypad, allow moisture ingress, and result in insulin over- or under-delivery, potentially causing hypoglycemia, hyperglycemia, or diabetic ketoacidosis..

Recalling firm: Medtronic MiniMed, Inc.
Classification: Class II
Status: Ongoing
Initiated: 2026-07-13
Firm location: Northridge, CA, United States

510(k) clearances named in this recall

1 on FDA's record

K251032 — MiniMed 780G insulin pumpMedtronic Minimed, Inc.·cleared 2025-07-01

K-numbers as listed on FDA's Recall Enterprise System record for this event (openFDA device/recall k_numbers). The recall may also cover devices cleared under other submissions not named here.

Product description

MiniMed 780G Insulin Pump, Model: MMT-1885CLW, MMT-1886CLW

Reason for recall

Loaner insulin pumps may have been cleaned with chemically incompatible products that could damage the pump case or keypad, allow moisture ingress, and result in insulin over- or under-delivery, potentially causing hypoglycemia, hyperglycemia, or diabetic ketoacidosis.

Data sourced from openFDA. This site is unofficial and independent of the FDA.