Is this FDA enforcement data for Kico Knee Innovation Company 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.

What is the most recent FDA action against Kico Knee Innovation Company?

The most recent FDA event Argus HQ has on file for Kico Knee Innovation Company is dated 2026-06-10, with a severity rating of "high" 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 Kico Knee Innovation Company 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 Kico Knee Innovation Company is observed, this page's event count and history update automatically.

Kico Knee Innovation Company — FDA Enforcement History

FDA action counts

Total FDA actions	2
Warning letters	0
Recalls	2
Approval records	0
Form 483 inspection citations	0
Most recent action	June 10, 2026

In short: Argus HQ has recorded 2 FDA events for Kico Knee Innovation Company: 0 warning letters, 2 recalls, 0 approvals, and 0 inspection 483 observations. These events span from 2026-06-10 to 2026-06-10. The most severe rating Argus HQ has assigned across this history is "high". 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. Kico Knee Innovation Company has 2 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.

Enforcement history

On 2026-06-10, Argus HQ recorded a FDA recall for Kico Knee Innovation Company, rated "high" severity in Argus HQ's classification: Kico Knee Innovation Company — Class II recall: Arvis Hip & Knee 2.0 Instrument Set, REF: IN-21200 containing one of the followi… An FDA recall record reflects a firm removing or correcting a product already in distribution because it does not meet FDA requirements. On 2026-06-10, Argus HQ recorded a FDA recall for Kico Knee Innovation Company, rated "high" severity in Argus HQ's classification: Kico Knee Innovation Company — Class II recall: Arvis Hip & Knee 3.0 Instrument Set, REF: IN-28000 containing one of the followi… An FDA recall record reflects a firm removing or correcting a product already in distribution because it does not meet FDA requirements. In total, Kico Knee Innovation Company has 2 FDA events on file with Argus HQ across the sources Argus HQ currently tracks (FDA Warning Letters, recalls, drug/biologic approvals, and Form 483 inspection observations). 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.

Frequently asked questions

Is this FDA enforcement data for Kico Knee Innovation Company 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 Kico Knee Innovation Company had?: Argus HQ has recorded 2 FDA events for Kico Knee Innovation Company: 0 warning letters, 2 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 Kico Knee Innovation Company?: The most recent FDA event Argus HQ has on file for Kico Knee Innovation Company is dated 2026-06-10, with a severity rating of "high" 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 Kico Knee Innovation Company 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 Kico Knee Innovation Company is observed, this page's event count and history update automatically.

Every FDA action tied to this company, the week it happens.

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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). Kico Knee Innovation Company — FDA Enforcement History. Digital Empire LLC. Retrieved from https://argushq.ai/company/kico-knee-innovation-company

MLA

"Kico Knee Innovation Company — FDA Enforcement History." Argus HQ Research, Digital Empire LLC, 2026, argushq.ai/company/kico-knee-innovation-company.

Chicago

Argus HQ Research. "Kico Knee Innovation Company — FDA Enforcement History." Digital Empire LLC. Accessed July 13, 2026. https://argushq.ai/company/kico-knee-innovation-company.

BibTeX

@misc{argushq_argushq_ai_company_kico_knee_innovation_company_2026,
  title = {Kico Knee Innovation Company — FDA Enforcement History},
  author = {{Argus HQ Research}},
  year = {2026},
  publisher = {Digital Empire LLC},
  url = {https://argushq.ai/company/kico-knee-innovation-company},
  note = {Accessed: July 13, 2026}
}

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