# FDA recall Z-0517-2021

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

## Product

MiniMed 630G with SmartGuard, insulin pump,  Ref/Model # MMT-1754K, MMT-1714K, MMT-1755K - Product Usage: intended for continuous delivery of basal insulin (at user selectable rates) and administration of insulin boluses (in user selectable amounts) for the management of diabetes mellitus in persons, fourteen years of age and older, 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-0517-2021
- **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-0517-2021

## Citation

> AI Analytics. FDA recall Z-0517-2021. Retrieved 2026-07-28 from https://api.ai-analytics.org/recall/Z-0517-2021. Source: US FDA. Licensed CC0.

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