---
title: "Medtronic: MiniMed™ 600 series or 700 series insulin pumps — FDA announcement Oct 18, 2024 | Is It on Recall"
description: "Device & Drug Safety - Defect"
url: https://isitonrecall.com/recall/fdapress-e20da1ce5038309b-medtronic-minimedtm-600-series-or-700-series-insulin-pumps/
updated: 2026-10-01
site: "Is It on Recall"
language: en
---

[Recall archive](https://isitonrecall.com/archives/) / FDA company announcement

# Medtronic: MiniMed™ 600 series or 700 series insulin pumps — FDA announcement Oct 18, 2024

Published notice; closure not supplied

A company announcement posted by FDA. The listing date can differ from the original announcement date. The absence of a termination marker does not prove the recall is currently ongoing.

Source date Oct 18, 2024. Retrieved Oct 1, 2026. Last updated Oct 1, 2026.

Archive changed Oct 1, 2026. USDA FSIS records are unavailable; [check FSIS directly](https://www.fsis.usda.gov/recalls). [Source coverage and dates](https://isitonrecall.com/sources/).

## What the record says

- **Product**: MiniMed™ 600 series or 700 series insulin pumps
- **Reason**: Device & Drug Safety - Defect
- **Classification**: Not supplied
- **Recalling firm**: Medtronic plc
- **Quantity**: Not supplied
- **Agency-reported status**: Company recall announcement
- **Source record identifier**: e20da1ce5038309b

[Open the official record](https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/voluntary-recall-notifying-medtronic-insulin-pump-users-potential-risks-shortened-pump-battery-life)

## Lot and product identifiers

| Label field | Details supplied by the agency |
| --- | --- |
| Lot, code or applicability | Not supplied |

Match all identifying details in the current notice. A brand name alone is not enough.

## Distribution

Not supplied

No US distribution state could be established from this record. Check the official notice.

## Dates in the source

- **Fda listing date**: Oct 18, 2024
- **Company announcement date**: Oct 4, 2024

FDA company pages use the listing date; enforcement records use initiation dates; CPSC uses recall date; NHTSA uses report-received date. These dates are not interchangeable.

## What to do next

Customers are being notified of the importance of checking built-in alerts and alarms for battery status and to contact Medtronic for pump replacement if affected by this issue Users should always carry an extra set of new AA lithium or alkaline batteries or fully charged NiMH batteries should they need to replace the battery sooner than expected. Users who notice a significant decrease in battery life from their usual experience, regardless of whether their pump has been dropped, bumped, or has experienced physical impact, should contact their local Medtronic team to determine whether a replacement pump is needed. Customers in the U.S. can call 1-800-378-2292 for 24-hour technical support. Customer outside the U.S. can click on this link to find the number for their local support team.

[Read the current instructions](https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/voluntary-recall-notifying-medtronic-insulin-pump-users-potential-risks-shortened-pump-battery-life)

## Related records

[Medical devices records](https://isitonrecall.com/category/medical-devices/) [Medtronic plc records](https://isitonrecall.com/brand/medtronic-plc/)