MiniMed Go App recall

For MiniMed Go app version 1.0.0 and 1.1.0, when the Set day and night is turned OFF and missed dose or Correct high glucose alerts are enabled, the associated alerts will not be triggered during the nighttime. This could result in missed rapid-acting insulin doses without the user s knowledge, and may lead to delayed therapy and an increased risk of hyperglycemia.

MiniMed Go App, Model: MMT-8600 (iOS), MMT-8601 (Android)

Quantity: 3,465

Check whether you have the product (match the lot numbers, dates or codes in the official notice). Stop using it, and return it or throw it away as the notice says.

Company

Medtronic MiniMed, Inc., Northridge, CA

Date

Wednesday, July 29

Severity

Class II
the product could cause temporary or reversible health problems.

Where sold

Nationwide
Worldwide - US Nationwide distribution in the states and territories of PR, OH, WA, IL, NC, PA, VA, MN, ID, CA, UT, MI, NJ, MS, SC, CO, AZ, OR, AR, MO, TX, AL, FL, NY, IN, TN, IA, WI, MA, LA, OK, GA, KS, NM, CT, KY, NH, NV, MD and the countries of Australia, Switzerland, Germany, Denmark, Spain, Fi…

Status

Ongoing

Recall number

Z-2778-2026

Source

U.S. Food and Drug Administration