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Recall Observatory FDA recall evidence

Device product

InPen App, Model/CFN Number: MMT-8061 (Android Users)

Z-0958-2026

November 13, 2025

Class II

Product summary

Firm
Medtronic MiniMed, Inc.
Event
Event 97904
Status
Ongoing
Classification
Class II
Quantity
8251
Official record key
device-enforcement:Z-0958-2026

Official wording

Reason: When app is uninstalled and reinstalled, insulin pen software issue causes Choose Notification Style Screen to not show during setup so users can't choose to allow notifications to override phone settings when on mute/Do Not Disturb, and previously set up override permission is deleted, so audible and vibratory notifications not received, which may lead to delayed insulin therapy, hyperglycemia.

Code information: Software Versions: 7.5.0, 7.5.1, and 8.0.0. UDI-DI: 00763000974596

Distribution pattern: US: IL, AZ, MN, NE, KS, TN, CA, FL, TX, WA, MO, NC, NY, WI, IN, ME, CT, RI, MD, PA, OK, KY, MA, DE, UT, ID, VA, MI, OH, LA, NJ, IA, MT, HI, AR, OR, SC, AL, CO, WY, VT, NV, GA, MS, SD, AK, WV, NH, ND, NM. OUS: Austria, Belgium, Chile, Czech Republic, Denmark, Egypt, Estonia, Finland, France, Georgia, Germany, Greece, Hungary, Iceland, Ireland, Israel, Italy, Luxembourg, Netherlands, Norway, Poland, Portugal, Romania, South Africa, Spain, Sweden, Switzerland, United Kingdom

Derived failure modes

  • Device software or design

    reason.device_software_design · v1.0.0

    software issue