How many FDA actions does Argus HQ track for SURGIFY MEDICAL OY?

19 total: 0 warning letters, 19 recalls, 0 approval records, and 0 Form 483 inspection citations.

What is the most recent FDA action on file for SURGIFY MEDICAL OY?

July 1, 2026. Argus HQ ingests new FDA enforcement records daily.

Has SURGIFY MEDICAL OY had product recalls?

Yes, 19 recalls on file. See the full history below for each one.

Is this FDA enforcement data for SURGIFY MEDICAL OY 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.

SURGIFY MEDICAL OY's Complete FDA Record

FDA action counts

Total FDA actions	19
Warning letters	0
Recalls	19
Approval records	0
Form 483 inspection citations	0
Most recent action	July 1, 2026

The short version: Argus HQ has recorded 19 FDA events for SURGIFY MEDICAL OY: 0 warning letters, 19 recalls, 0 approvals, and 0 inspection 483 observations. These events span from 2026-07-01 to 2026-07-01. 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. SURGIFY MEDICAL OY has 19 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.

Enforcement history

On 2026-07-01, Argus HQ recorded a FDA recall for SURGIFY MEDICAL OY, rated "high" severity in Argus HQ's classification: SURGIFY MEDICAL OY — Class II recall: Surgify Halo, 4.0 mm, Extendable, Model/Catalog Number: 40.000.SEE.H1; drills, b… An FDA recall record reflects a firm removing or correcting a product already in distribution because it does not meet FDA requirements. On 2026-07-01, Argus HQ recorded a FDA recall for SURGIFY MEDICAL OY, rated "high" severity in Argus HQ's classification: SURGIFY MEDICAL OY — Class II recall: Surgify Halo, 4.0 mm, Short, Model/Catalog Number: 40.125.NVG.H1; drills, burrs,… An FDA recall record reflects a firm removing or correcting a product already in distribution because it does not meet FDA requirements. On 2026-07-01, Argus HQ recorded a FDA recall for SURGIFY MEDICAL OY, rated "high" severity in Argus HQ's classification: SURGIFY MEDICAL OY — Class II recall: Surgify Halo, 4.0 mm, Short, Model/Catalog Number: 40.070.NVG.U1; drills, burrs,… An FDA recall record reflects a firm removing or correcting a product already in distribution because it does not meet FDA requirements. On 2026-07-01, Argus HQ recorded a FDA recall for SURGIFY MEDICAL OY, rated "high" severity in Argus HQ's classification: SURGIFY MEDICAL OY — Class II recall: Surgify Halo, 5.4 mm, Long, Model/Catalog Number: 54.140.SHD.H1; drills, burrs,… An FDA recall record reflects a firm removing or correcting a product already in distribution because it does not meet FDA requirements. On 2026-07-01, Argus HQ recorded a FDA recall for SURGIFY MEDICAL OY, rated "high" severity in Argus HQ's classification: SURGIFY MEDICAL OY — Class II recall: Surgify Halo, 5.4 mm, Extendable, Model/Catalog Number: 54.000.SEE.U1; drills, b… An FDA recall record reflects a firm removing or correcting a product already in distribution because it does not meet FDA requirements. On 2026-07-01, Argus HQ recorded a FDA recall for SURGIFY MEDICAL OY, rated "high" severity in Argus HQ's classification: SURGIFY MEDICAL OY — Class II recall: Surgify Halo, 5.4 mm, Short, Model/Catalog Number: 54.070.NVG.H1; drills, burrs,… An FDA recall record reflects a firm removing or correcting a product already in distribution because it does not meet FDA requirements. On 2026-07-01, Argus HQ recorded a FDA recall for SURGIFY MEDICAL OY, rated "high" severity in Argus HQ's classification: SURGIFY MEDICAL OY — Class II recall: Surgify Halo, 3.0 mm, Long, Model/Catalog Number: 30.125.NVG.U2; drills, burrs,… An FDA recall record reflects a firm removing or correcting a product already in distribution because it does not meet FDA requirements. On 2026-07-01, Argus HQ recorded a FDA recall for SURGIFY MEDICAL OY, rated "high" severity in Argus HQ's classification: SURGIFY MEDICAL OY — Class II recall: Surgify Halo, 4.0 mm, Extendable, Model/Catalog Number: 40.000.SEE.U1; drills, b… An FDA recall record reflects a firm removing or correcting a product already in distribution because it does not meet FDA requirements. On 2026-07-01, Argus HQ recorded a FDA recall for SURGIFY MEDICAL OY, rated "high" severity in Argus HQ's classification: SURGIFY MEDICAL OY — Class II recall: Surgify Halo, 5.4 mm, Long, Model/Catalog Number: 54.125.NVG.H1; drills, burrs,… An FDA recall record reflects a firm removing or correcting a product already in distribution because it does not meet FDA requirements. On 2026-07-01, Argus HQ recorded a FDA recall for SURGIFY MEDICAL OY, rated "high" severity in Argus HQ's.

Frequently asked questions

How many FDA actions does Argus HQ track for SURGIFY MEDICAL OY?: 19 total: 0 warning letters, 19 recalls, 0 approval records, and 0 Form 483 inspection citations.
What is the most recent FDA action on file for SURGIFY MEDICAL OY?: July 1, 2026. Argus HQ ingests new FDA enforcement records daily.
Has SURGIFY MEDICAL OY had product recalls?: Yes, 19 recalls on file. See the full history below for each one.
Is this FDA enforcement data for SURGIFY MEDICAL OY 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.

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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). SURGIFY MEDICAL OY's Complete FDA Record. Digital Empire LLC. Retrieved from https://argushq.ai/company/surgify-medical-oy

MLA

"SURGIFY MEDICAL OY's Complete FDA Record." Argus HQ Research, Digital Empire LLC, 2026, argushq.ai/company/surgify-medical-oy.

Chicago

Argus HQ Research. "SURGIFY MEDICAL OY's Complete FDA Record." Digital Empire LLC. Accessed July 13, 2026. https://argushq.ai/company/surgify-medical-oy.

BibTeX

@misc{argushq_argushq_ai_company_surgify_medical_oy_2026,
  title = {SURGIFY MEDICAL OY's Complete FDA Record},
  author = {{Argus HQ Research}},
  year = {2026},
  publisher = {Digital Empire LLC},
  url = {https://argushq.ai/company/surgify-medical-oy},
  note = {Accessed: July 13, 2026}
}

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