# FDA recall Z-0518-2021

> **Medtronic Inc.** · Class II · device recall initiated 2020-04-30.

## Product

MiniMed 640G, insulin pump, Ref/Model # MMT-1711K, MMT-1752K, MMT-1752, Rx Only - Product Usage: indicated for the continuous delivery of insulin, at set and variable rates, for the management of diabetes mellitus in persons requiring insulin.

## Reason for recall

Missing solder battery connection, which could interrupt power of insulin pump.

## Distribution

Worldwide distribution - U.S. Nationwide Distribution in the state of MD and the countries of Canada, Netherlands, Norway. ***Model 630G distributed in Canada and Model 670G distributed in US ***MODEL640G Distributed OUS ONLY***  OUS: Australia, Canada, Netherlands and Norway.

## Key facts

- **Recall number:** Z-0518-2021
- **Recalling firm:** Medtronic Inc.
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2020-04-30
- **Report date:** 2020-12-09

- **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-0518-2021

## Citation

> AI Analytics. FDA recall Z-0518-2021. Retrieved 2026-07-26 from https://api.ai-analytics.org/recall/Z-0518-2021. Source: US FDA. Licensed CC0.

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