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 2026-04-01; 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: MiniMed" 780G - MMT-1884 MiniMed" 780G - MMT-1886 With Software 6.60 and 6.6…

Name: FDA Recall Record — Medtronic MiniMed, Inc.
Creator: Argus HQ
Published: 2026-04-01
License: https://argushq.ai/methodology

Event date: 2026-04-01 00:00:00Z
Observed: 2026-07-16 23:20:07Z
Source ID: Z-1635-2026
Payload hash: 1d6e0e353482abf87ddc3c43…

Summary

Three software defects (Pump Error 53, BG check, and Critical Pump Error (Open Book Image)) that occurred as a result of software updates (versions 6.60, 6.61, and 6.62), which could result in a risk of hypoglycemia or hyperglycemia due to inaccuracies in insulin delivery (either under-delivery, ov… 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 2026-04-01; 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: MiniMed" 780G - MMT-1884  MiniMed" 780G - MMT-1886    With Software 6.60 and 6.6…. Digital Empire Holdings LLC. Retrieved from https://argushq.ai/events/fda-recall-medtronic-minimed-inc-z-1635-2026

MLA

"Medtronic MiniMed, Inc. — Class II recall: MiniMed" 780G - MMT-1884  MiniMed" 780G - MMT-1886    With Software 6.60 and 6.6…." Argus HQ Research, Digital Empire Holdings LLC, 2026, argushq.ai/events/fda-recall-medtronic-minimed-inc-z-1635-2026.

Chicago

Argus HQ Research. "Medtronic MiniMed, Inc. — Class II recall: MiniMed" 780G - MMT-1884  MiniMed" 780G - MMT-1886    With Software 6.60 and 6.6…." Digital Empire Holdings LLC. Accessed July 23, 2026. https://argushq.ai/events/fda-recall-medtronic-minimed-inc-z-1635-2026.

BibTeX

@misc{argushq_argushq_ai_events_fda_recall_medtronic_minimed_inc_z_1635_2026_2026,
  title = {Medtronic MiniMed, Inc. — Class II recall: MiniMed" 780G - MMT-1884  MiniMed" 780G - MMT-1886    With Software 6.60 and 6.6…},
  author = {{Argus HQ Research}},
  year = {2026},
  publisher = {Digital Empire Holdings LLC},
  url = {https://argushq.ai/events/fda-recall-medtronic-minimed-inc-z-1635-2026},
  note = {Accessed: July 23, 2026}
}

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