MiniMed 670G Insulin Pump, Model: MMT-1781, MMT-1782 recallZ-2981-2026 · Medtronic MiniMed, Inc. · initiated Jul 13, 2026
Class II Open, Classified All recalls posted in August 2026
Is my device affected?
- Compare the model, catalog and lot or serial numbers on your device or its packaging with the code information below. A recall usually covers only specific models or lots.
- If yours is listed, follow the instructions from Medtronic MiniMed, Inc. or your healthcare provider. The company's action is summarized under what the company is doing.
- Do not stop using a prescribed or implanted device on your own — talk to your healthcare provider first.
Where to find your model and lot numbers · What recall classes and statuses mean
Why it was recalled
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.
FDA root cause category: Process design
What the company is doing
On 7/13/2026, field safety notices were sent to customers asking them to do the following: 1) Stop using the loaner pump and contact the firm to arrange for loaner pump return. 2) Contact your Healthcare Professional (HCP) to ensure you have access to backup insulin therapy supplies or alternative plans, which may include short- and long-acting insulins, syringes, with dosage instructions from your HCP. 3) Complete and return the customer acknowledgement form. Questions can be directed to the firm's Tech Support: 1-800-646-4633
Recall details
- Recall number
- Z-2981-2026
- Recall class
- Class II
- Status
- Open, Classified
- Initiated by the company
- Jul 13, 2026
- Posted by the FDA
- Aug 18, 2026
- Recalling firm
- Medtronic MiniMed, Inc.
- Quantity
- 7
- Product code
- OZP
- FDA submissions
- P160017
- Distribution
- International distribution to the countries of Germany, Denmark, Austria, Netherlands, United Kingdom, Italy, Belgium, Ireland, Switzerland, Sweden, Northern Ireland.
Product description
MiniMed 670G Insulin Pump, Model: MMT-1781, MMT-1782;
Code information (models, lots, serial numbers)
Model/UDI-DI Serial Numbers: MMT-1781/00763000404536/NG2665223H, NG2748200H, NG2748664H, NG2755237H, NG2716176H, NG3547582H. MMT-1782/00763000404543/NG2768190H
Other devices under the same FDA submission
75 devices cleared under P160017 — the recall does not name any of them by identifier. One submission often covers many models, so they may or may not be affected.
- MiniMed® 670G MMT-1780KPKMedtronic Minimed, Inc. · Artificial pancreas device system, single hormonal control3 recalls78 deaths55,723 reports
- MiniMed® 670G MMT-1780KPKMedtronic Minimed, Inc. · Automated insulin dosing device system, single hormonal control2 recalls51 deaths33,713 reports
- MiniMed®670G MMT-1780KPKMedtronic Minimed, Inc. · Artificial pancreas device system, single hormonal control3 recalls39 deaths28,789 reports
- MiniMed® 670G MMT-1780KLMedtronic Minimed, Inc. · Automated insulin dosing device system, single hormonal control3 recalls8 deaths8,353 reports
- MiniMed® 670G MMT-1780KMedtronic Minimed, Inc. · Artificial pancreas device system, single hormonal control3 recalls7 deaths6,776 reports
- MiniMed® 670G MMT-1780KPKMedtronic Minimed, Inc. · Automated insulin dosing device system, single hormonal control3 recalls10 deaths4,325 reports
- Guardian™ Sensor (3) MMT-7020AMedtronic Minimed, Inc. · Automated insulin dosing device system, single hormonal control1,304 reports
- MiniMed® 670G MMT-1780KLMedtronic Minimed, Inc. · Artificial pancreas device system, single hormonal control3 recalls1 death958 reports
- Enlite ® MMT-7008AMedtronic Minimed, Inc. · Automated insulin dosing , threshold suspend994 reports
- MiniMed® 670G MMT-1780KLMedtronic Minimed, Inc. · Automated insulin dosing device system, single hormonal control3 recalls2 deaths783 reports
- MiniMed® 630G MMT-1715KMedtronic Minimed, Inc. · Automated insulin dosing device system, single hormonal control3 recalls8 deaths781 reports
- MiniMed® 670G MMT-1780KLMedtronic Minimed, Inc. · Automated insulin dosing device system, single hormonal control2 recalls1 death823 reports
Sources and updates
- Recall record: FDA Medical Device Recalls, file dated Oct 16, 2026 · View the FDA recall notice ↗
- Devices: FDA GUDID, file dated Oct 13, 2026. Devices are linked when their identifier (with a valid check digit) appears in the recall's code information.
- Page last rebuilt: Oct 18, 2026. Text above is shown as published by the FDA.
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