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 2026-04-08; 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: Paradigm Insulin Pump (MMT-712, MMT-715)

Name: FDA Recall Record — Medtronic MiniMed, Inc.
Creator: Argus HQ
Published: 2026-04-08
License: https://argushq.ai/methodology

Event date: 2026-04-08 00:00:00Z
Observed: 2026-07-16 23:20:07Z
Source ID: Z-1748-2026
Payload hash: acf2122fa379c931871fb9e6…

Summary

All Medtronic MiniMed infusion pumps (Paradigm series, 600 series, and BLE 700 series) were found to be affected by unintended over- and under-delivery of insulin when the pump is elevated or lowered relative to the infusion site, respectively, because of changes in gravitational force impacting hyd… 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 2026-04-08; 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 (2026). Medtronic MiniMed, Inc. — Class II recall: Paradigm Insulin Pump (MMT-712, MMT-715). Digital Empire Holdings LLC. Retrieved from https://argushq.ai/events/fda-recall-medtronic-minimed-inc-z-1748-2026

MLA

"Medtronic MiniMed, Inc. — Class II recall: Paradigm Insulin Pump (MMT-712, MMT-715)." Argus HQ Research, Digital Empire Holdings LLC, 2026, argushq.ai/events/fda-recall-medtronic-minimed-inc-z-1748-2026.

Chicago

Argus HQ Research. "Medtronic MiniMed, Inc. — Class II recall: Paradigm Insulin Pump (MMT-712, MMT-715)." Digital Empire Holdings LLC. Accessed July 23, 2026. https://argushq.ai/events/fda-recall-medtronic-minimed-inc-z-1748-2026.

BibTeX

@misc{argushq_argushq_ai_events_fda_recall_medtronic_minimed_inc_z_1748_2026_2026,
  title = {Medtronic MiniMed, Inc. — Class II recall: Paradigm Insulin Pump (MMT-712, MMT-715)},
  author = {{Argus HQ Research}},
  year = {2026},
  publisher = {Digital Empire Holdings LLC},
  url = {https://argushq.ai/events/fda-recall-medtronic-minimed-inc-z-1748-2026},
  note = {Accessed: July 23, 2026}
}

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