CLASS II ONGOING Device recall · Reported 26 Aug 2026 · FDA Enforcement Report

MiniMed Insulin Pump recalled by Medtronic MiniMed

Medtronic MiniMed is recalling MiniMed Insulin Pump, distributed nationwide in the US. The recall was initiated on 13 Jul 2026 and the FDA has classified it as Class II.

Check your package

Lot, batch or date codesModel/UDI-DI Serial Numbers: MMT-1781/00763000404536/NG2665223H, NG2748200H, NG2748664H, NG2755237H, NG2716176H, NG3547582H. MMT-1782/00763000404543/NG2768190H

Quantity recalled7

Stop using the device if the notice says to, and contact the manufacturer or your healthcare provider for the correction or replacement.

Recall details

Recall number: Z-2981-2026
FDA event ID: 99374
Recalling firm: Medtronic MiniMed, Northridge, CA
Classification: Class II
Status: Ongoing
Recall initiated: 13 Jul 2026
FDA classified: 18 Aug 2026
Reported: 26 Aug 2026
Type: Voluntary: Firm initiated
Reason category: Other Reasons
Device type: Insulin Pumps & Glucose Monitors

Timeline

13 Jul 2026	Recall initiated by company
18 Aug 2026	Classified by FDA	+36 days
26 Aug 2026	Published in enforcement report	+8 days

Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.

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.

Product as listed by the FDA

MiniMed 670G Insulin Pump, Model: MMT-1781, MMT-1782;

Where it was distributed

International distribution to the countries of Germany, Denmark, Austria, Netherlands, United Kingdom, Italy, Belgium, Ireland, Switzerland, Sweden, Northern Ireland.

Nationwide

Questions about this recall

Is MiniMed Insulin Pump recalled?

Yes. Medtronic MiniMed recalled MiniMed Insulin Pump on 13 Jul 2026. The recall is Class II and its status is Ongoing. Recall number Z-2981-2026.

Why was it recalled?

Which lots are affected?

Model/UDI-DI Serial Numbers: MMT-1781/00763000404536/NG2665223H, NG2748200H, NG2748664H, NG2755237H, NG2716176H, NG3547582H. MMT-1782/00763000404543/NG2768190H

Where was it sold?

International distribution to the countries of Germany, Denmark, Austria, Netherlands, United Kingdom, Italy, Belgium, Ireland, Switzerland, Sweden, Northern Ireland.

What should I do if I have it?

Stop using the device if the notice says to, and contact the manufacturer or your healthcare provider for the correction or replacement.

What does Class II mean?

Class II means the product may cause temporary or medically reversible health problems, or the probability of serious harm is remote.

Read the official FDA notice · Source record retrieved 21 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.

More recalls from Medtronic MiniMed

All 78

Reported	Class	Recall	Company	Reason	Where
26 Aug 2026Device	CLASS II	MiniMed Insulin Pump recalled by Medtronic MiniMed	Medtronic MiniMed	Other	Nationwide
26 Aug 2026Device	CLASS II	MiniMed Insulin Pump recalled by Medtronic MiniMed	Medtronic MiniMed	Other	Nationwide
29 Jul 2026Device	CLASS II	MiniMed Go App recalled by Medtronic MiniMed	Medtronic MiniMed	Lead & Heavy Metals	Nationwide
15 Jul 2026Device	CLASS II	MiniMed Insulin Pump recalled by Medtronic MiniMed	Medtronic MiniMed	Lead & Heavy Metals	Nationwide
8 Apr 2026Device	CLASS II	MiniMed Insulin Pump (Mmt-1760, Mmt-1761, Mmt recalled	Medtronic MiniMed	Other	Nationwide

Other Insulin Pumps & Glucose Monitors recalls

All 459

Reported	Class	Recall	Company	Reason	Where
26 Aug 2026Device	CLASS II	MiniMed Insulin Pump recalled by Medtronic MiniMed	Medtronic MiniMed	Other	Nationwide
26 Aug 2026Device	CLASS II	MiniMed Insulin Pump recalled by Medtronic MiniMed	Medtronic MiniMed	Other	Nationwide
15 Jul 2026Device	CLASS II	MiniMed Insulin Pump recalled by Medtronic MiniMed	Medtronic MiniMed	Lead & Heavy Metals	Nationwide
8 Jul 2026Device	CLASS I	Omnipod (Eros) Pod recalled by Insulet	Insulet	Lead & Heavy Metals	Nationwide
8 Jul 2026Device	CLASS I	Omnipod DASH Pod recalled by Insulet	Insulet	Lead & Heavy Metals	Nationwide