# FDA recall Z-2981-2026

> **Medtronic MiniMed, Inc.** · Class II · device recall initiated 2026-07-13.

## Product

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

## 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.

## Distribution

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

## Key facts

- **Recall number:** Z-2981-2026
- **Recalling firm:** Medtronic MiniMed, Inc.
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2026-07-13
- **Report date:** 2026-08-26

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Northridge, CA, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-2981-2026

## Citation

> MORVS. FDA recall Z-2981-2026. Retrieved 2026-10-17 from https://api.morvs.ai/recall/Z-2981-2026. Source: US FDA. Licensed CC0.

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