Medtronic Inc. recalls MiniMed 670G, insulin pump, Ref/Model # MMT-1760KPK, MMT-1762KCN, MMT-1762WWK - Product Usage: indicated for continuous

Recalled December 9, 2020 · FDA recall Z-0516-2021 · Medtronic

Hazard

Missing solder battery connection, which could interrupt power of insulin pump. · FDA Class II

Units

391

Sold at

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.

Description

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

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.

Manufacturer(s)

Medtronic Inc.

Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →