# FDA recall Z-2698-2026

> **Medtronic MiniMed, Inc.** · Class II · device recall initiated 2026-05-27.

## Product

MiniMed 780G Insulin Pump, REF: MMT-1885, MMT-1886, MMT-1895, MMT-1896

## Reason for recall

A software anomaly can occur when the pump is paired with the Instinct sensor. Under certain circumstances, the pump unexpectedly stops delivering insulin and displays two error messages back-to-back: Pump Error 53 followed immediately by Pump Error 23. Insulin delivery will stop which may lead to delayed therapy and an increased risk of hyperglycemia or diabetic ketoacidosis (DKA).

## Distribution

International distribution to the countries of Spain, Great Britain, Netherlands, Italy.

## Key facts

- **Recall number:** Z-2698-2026
- **Recalling firm:** Medtronic MiniMed, Inc.
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2026-05-27
- **Report date:** 2026-07-15

- **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-2698-2026

## Citation

> MORVS. FDA recall Z-2698-2026. Retrieved 2026-10-21 from https://api.morvs.ai/recall/Z-2698-2026. Source: US FDA. Licensed CC0.

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