# FDA recall Z-0516-2021

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

## Product

MiniMed 670G, insulin pump, Ref/Model # MMT-1760KPK, MMT-1762KCN, MMT-1762WWK - Product Usage: indicated for continuous or periodic monitoring of glucose levels in the fluid under the skin, and detecting possible low and high glucose episodes. When using a sensor and transmitter, the pump displays continuous sensor glucose values and stores this data so that it can be analyzed to track patterns and improve diabetes management. This data can be uploaded to a computer for analysis of historical glucose values.

## 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-0516-2021
- **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-0516-2021

## Citation

> AI Analytics. FDA recall Z-0516-2021. Retrieved 2026-07-26 from https://api.ai-analytics.org/recall/Z-0516-2021. Source: US FDA. Licensed CC0.

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