Is this FDA enforcement data for Medtronic MiniMed, Inc. official?

Every record links directly to its primary FDA.gov source. Argus HQ aggregates and structures public FDA data; the verbatim FDA record is always the source of truth.

How many FDA actions has Medtronic MiniMed, Inc. had?

Argus HQ has recorded 37 FDA events for Medtronic MiniMed, Inc.: 0 warning letters, 37 recalls, 0 approvals, and 0 Form 483 inspection observations. Argus HQ ingests these records directly from FDA's own public enforcement and approval databases rather than from company disclosures.

What is the most recent FDA action against Medtronic MiniMed, Inc.?

The most recent FDA event Argus HQ has on file for Medtronic MiniMed, Inc. is dated 2026-04-08, with a severity rating of "critical" in Argus HQ's classification. Argus HQ ingests these records directly from FDA's own public enforcement and approval databases rather than from company disclosures.

Does Argus HQ track new FDA actions for Medtronic MiniMed, Inc. automatically?

Yes. Argus HQ ingests FDA sources daily, including FDA warning letters, recalls, drug and biologic approvals, and Form 483 inspection observations. When a new FDA action linked to Medtronic MiniMed, Inc. is observed, this page's event count and history update automatically.

Medtronic MiniMed, Inc. — FDA Enforcement History

FDA action counts

Total FDA actions	37
Warning letters	0
Recalls	37
Approval records	0
Form 483 inspection citations	0
Most recent action	April 8, 2026

In short: Argus HQ has recorded 37 FDA events for Medtronic MiniMed, Inc.: 0 warning letters, 37 recalls, 0 approvals, and 0 inspection 483 observations. These events span from 2024-02-14 to 2026-04-08. The most severe rating Argus HQ has assigned across this history is "critical". Argus HQ ingests these records directly from FDA's own public enforcement and approval databases rather than from company disclosures. This page reflects only the FDA event types Argus HQ currently tracks -- FDA Warning Letters, recalls, drug and biologic approvals, and Form 483 inspection observations -- and will update automatically as new FDA records are observed. Argus HQ ingests these records directly from FDA's own public enforcement and approval databases rather than from company disclosures. This page reflects only the FDA event types Argus HQ currently tracks -- FDA Warning Letters, recalls, drug and biologic approvals, and Form 483 inspection observations -- and will update automatically as new FDA records are observed.

Risk pattern analysis

Argus HQ analysis — not an FDA finding

This section is Argus HQ analysis, not an FDA finding. Medtronic MiniMed, Inc. has 37 separate FDA recalls on file, more than a single isolated recall event. A pattern across multiple FDA touchpoints does not by itself establish that any specific product currently poses a risk; it reflects only the frequency of FDA engagement with this company as recorded in Argus HQ's database. Argus HQ ingests these records directly from FDA's own public enforcement and approval databases rather than from company disclosures. This page reflects only the FDA event types Argus HQ currently tracks -- FDA Warning Letters, recalls, drug and biologic approvals, and Form 483 inspection observations -- and will update automatically as new FDA records are observed. Argus HQ does not independently verify FDA's underlying findings; this page summarizes what FDA has published and links back to the original FDA source for each event. Argus HQ ingests these records directly from FDA's own public enforcement and approval databases rather than from company disclosures.

Enforcement history

On 2026-04-08, Argus HQ recorded an FDA recall for Medtronic MiniMed, Inc., rated "high" severity in Argus HQ's classification: Medtronic MiniMed, Inc. — Class II recall: MiniMed 720G Insulin Pump (MMT-1809, MMT-1810, MMT-1859, MMT-1860, MMT-1867). On 2026-04-08, Argus HQ recorded an FDA recall for Medtronic MiniMed, Inc., rated "high" severity in Argus HQ's classification: Medtronic MiniMed, Inc. — Class II recall: MiniMed 670G Insulin Pump (MMT-1760, MMT-1761, MMT-1762, MMT-1780, MMT-1781, MMT…. On 2026-04-08, Argus HQ recorded an FDA recall for Medtronic MiniMed, Inc., rated "high" severity in Argus HQ's classification: Medtronic MiniMed, Inc. — Class II recall: MiniMed 780G Insulin Pump (MMT-1884, MMT-1885, MMT-1886, MMT-1894, MMT-1895, MMT…. On 2026-04-08, Argus HQ recorded an FDA recall for Medtronic MiniMed, Inc., rated "high" severity in Argus HQ's classification: Medtronic MiniMed, Inc. — Class II recall: Paradigm REAL-Time Insulin Pump (MMT-522, MMT-722). On 2026-04-08, Argus HQ recorded an FDA recall for Medtronic MiniMed, Inc., rated "high" severity in Argus HQ's classification: Medtronic MiniMed, Inc. — Class II recall: MiniMed 530G Insulin Pump (MMT-551, MMT-751). On 2026-04-08, Argus HQ recorded an FDA recall for Medtronic MiniMed, Inc., rated "high" severity in Argus HQ's classification: Medtronic MiniMed, Inc. — Class II recall: Paradigm REAL-Time Revel Insulin Pump (MMT-523, MMT-723). On 2026-04-08, Argus HQ recorded an FDA recall for Medtronic MiniMed, Inc., rated "high" severity in Argus HQ's classification: Medtronic MiniMed, Inc. — Class II recall: MiniMed 640G Insulin Pump (MMT-1711, MMT-1712, MMT-1751, MMT-1752). On 2026-04-08, Argus HQ recorded an FDA recall for Medtronic MiniMed, Inc., rated "high" severity in Argus HQ's classification: Medtronic MiniMed, Inc. — Class II recall: MiniMed 740G Insulin Pump (MMT-1811, MMT-1812, MMT-1861, MMT-1862). On 2026-04-08, Argus HQ recorded an FDA recall for Medtronic MiniMed, Inc., rated "high" severity in Argus HQ's classification: Medtronic MiniMed, Inc. — Class II recall: MiniMed 770G Insulin Pump (MMT-1880, MMT-1881, MMT-1882, MMT-1890, MMT-1891, MMT…. On 2026-04-08, Argus HQ recorded an FDA recall for Medtronic MiniMed, Inc., rated "high" severity in Argus HQ's classification: Medtronic MiniMed, Inc. — Class II recall: Paradigm Insulin Pump (MMT-712, MMT-715). On 2026-04-08, Argus HQ recorded an FDA recall for Medtronic MiniMed, Inc., rated "high" severity in Argus HQ's classification: Medtronic MiniMed, Inc. — Class II recall: Paradigm REAL-Time Veo Insulin Pump (MMT-554, MMT-754). On 2026-04-08, Argus HQ recorded an FDA recall for Medtronic MiniMed, Inc., rated "high" severity in Argus HQ's classification: Medtronic MiniMed, Inc. — Class II recall: MiniMed 700G Insulin Pump (MMT-1801, MMT-1805, MMT-1850, MMT-1851).

Frequently asked questions

Is this FDA enforcement data for Medtronic MiniMed, Inc. official?: Every record links directly to its primary FDA.gov source. Argus HQ aggregates and structures public FDA data; the verbatim FDA record is always the source of truth.
How many FDA actions has Medtronic MiniMed, Inc. had?: Argus HQ has recorded 37 FDA events for Medtronic MiniMed, Inc.: 0 warning letters, 37 recalls, 0 approvals, and 0 Form 483 inspection observations. Argus HQ ingests these records directly from FDA's own public enforcement and approval databases rather than from company disclosures.
What is the most recent FDA action against Medtronic MiniMed, Inc.?: The most recent FDA event Argus HQ has on file for Medtronic MiniMed, Inc. is dated 2026-04-08, with a severity rating of "critical" in Argus HQ's classification. Argus HQ ingests these records directly from FDA's own public enforcement and approval databases rather than from company disclosures.
Does Argus HQ track new FDA actions for Medtronic MiniMed, Inc. automatically?: Yes. Argus HQ ingests FDA sources daily, including FDA warning letters, recalls, drug and biologic approvals, and Form 483 inspection observations. When a new FDA action linked to Medtronic MiniMed, Inc. is observed, this page's event count and history update automatically.

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

Verified from FDA.gov · Last updated: Apr 8, 2026

Cite this record

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

APA

Argus HQ Research (2026). Medtronic MiniMed, Inc. — FDA Enforcement History. Digital Empire Holdings LLC. Retrieved from https://argushq.ai/company/medtronic-minimed-inc

MLA

"Medtronic MiniMed, Inc. — FDA Enforcement History." Argus HQ Research, Digital Empire Holdings LLC, 2026, argushq.ai/company/medtronic-minimed-inc.

Chicago

Argus HQ Research. "Medtronic MiniMed, Inc. — FDA Enforcement History." Digital Empire Holdings LLC. Accessed July 17, 2026. https://argushq.ai/company/medtronic-minimed-inc.

BibTeX

@misc{argushq_argushq_ai_company_medtronic_minimed_inc_2026,
  title = {Medtronic MiniMed, Inc. — FDA Enforcement History},
  author = {{Argus HQ Research}},
  year = {2026},
  publisher = {Digital Empire Holdings LLC},
  url = {https://argushq.ai/company/medtronic-minimed-inc},
  note = {Accessed: July 17, 2026}
}

Source: FDA.gov (aggregated across Warning Letters, Recalls, Approvals, Form 483s) ↗