Device recall

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

FDA recall source

Recall number

Z-2981-2026

Event id

99374

Status

Ongoing

FDA classification

Class II

Recalling firm

Medtronic MiniMed, Inc.

Report date

Aug 26, 2026

Posted

Aug 18, 2026

Initiated

Jul 13, 2026

Center classification date

Aug 18, 2026

Product code

OZP

Device type

Automated Insulin Dosing Device System, Single Hormonal Control

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.

Root cause

Process design

Quantity

7

Code info

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

Distribution

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

Voluntary or mandated

Voluntary: Firm initiated

Location

Northridge, CA, United States