Has Medtronic MiniMed, Inc. had other FDA enforcement actions?

Yes. Argus HQ has recorded 38 total FDA actions tied to Medtronic MiniMed, Inc.: 0 warning letters, 38 recalls, 0 approval records, and 0 Form 483 inspection citations.

What kind of FDA record is this?

This is an Argus HQ record of a FDA Recall, tagged high severity by Argus HQ. FDA published the underlying record on 2025-12-03; Argus observed and indexed it on 2026-07-16.

Where can I verify this record directly with FDA?

The verbatim FDA source record is the source of truth — Argus HQ links directly to it below. Always confirm against fda.gov before acting.

.hq

fda_recall · device_recall · high

Medtronic MiniMed, Inc. — Class II recall: CareLink Clinic, REF: MMT-7350

Name: FDA Recall Record — Medtronic MiniMed, Inc.
Creator: Argus HQ
Published: 2025-12-03
License: https://argushq.ai/methodology

Event date: 2025-12-03 00:00:00Z
Observed: 2026-07-16 23:20:07Z
Source ID: Z-0594-2026
Payload hash: 30ef84fcd3e9b6029d5c0c53…

Summary

Software error causing incorrect data to be displayed on the 24-hour Sensor Glucose Overview Graph, any potential therapy decisions were made based on the incorrect data displayed on the 24-hour sensor glucose overview graph may lead to hypoglycemia or hyperglycemia. Status: Ongoing.

Entities

Medtronic MiniMed, Inc.

View source record ↗

Frequently asked questions

Has Medtronic MiniMed, Inc. had other FDA enforcement actions?: Yes. Argus HQ has recorded 38 total FDA actions tied to Medtronic MiniMed, Inc.: 0 warning letters, 38 recalls, 0 approval records, and 0 Form 483 inspection citations.
What kind of FDA record is this?: This is an Argus HQ record of a FDA Recall, tagged high severity by Argus HQ. FDA published the underlying record on 2025-12-03; Argus observed and indexed it on 2026-07-16.
Where can I verify this record directly with FDA?: The verbatim FDA source record is the source of truth — Argus HQ links directly to it below. Always confirm against fda.gov before acting.

Compiled by Argus HQ Research from FDA primary sources · Reviewed by Andy Gaber, Founder

Cite this record

Reusing this data in reporting or research? Here’s a ready-made citation.

APA

Argus HQ Research (2025). Medtronic MiniMed, Inc. — Class II recall: CareLink Clinic, REF: MMT-7350. Digital Empire Holdings LLC. Retrieved from https://argushq.ai/events/fda-recall-medtronic-minimed-inc-z-0594-2026

MLA

"Medtronic MiniMed, Inc. — Class II recall: CareLink Clinic, REF: MMT-7350." Argus HQ Research, Digital Empire Holdings LLC, 2025, argushq.ai/events/fda-recall-medtronic-minimed-inc-z-0594-2026.

Chicago

Argus HQ Research. "Medtronic MiniMed, Inc. — Class II recall: CareLink Clinic, REF: MMT-7350." Digital Empire Holdings LLC. Accessed July 23, 2026. https://argushq.ai/events/fda-recall-medtronic-minimed-inc-z-0594-2026.

BibTeX

@misc{argushq_argushq_ai_events_fda_recall_medtronic_minimed_inc_z_0594_2026_2025,
  title = {Medtronic MiniMed, Inc. — Class II recall: CareLink Clinic, REF: MMT-7350},
  author = {{Argus HQ Research}},
  year = {2025},
  publisher = {Digital Empire Holdings LLC},
  url = {https://argushq.ai/events/fda-recall-medtronic-minimed-inc-z-0594-2026},
  note = {Accessed: July 23, 2026}
}

Informational only. Not legal, financial, or medical advice.