What is the most recent FDA action on file for ConMed Corporation?

June 24, 2026. Argus HQ ingests new FDA enforcement records daily.

Has ConMed Corporation had product recalls?

Yes, 11 recalls on file. See the full history below for each one.

Is this FDA enforcement data for ConMed Corporation 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 ConMed Corporation had?

Argus HQ has recorded 11 FDA events for ConMed Corporation: 0 warning letters, 11 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.

FDA Actions Against ConMed Corporation

At a glance: Argus HQ has recorded 11 FDA events for ConMed Corporation: 0 warning letters, 11 recalls, 0 approvals, and 0 inspection 483 observations. These events span from 2026-06-24 to 2026-06-24. 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.

FDA action counts

Total FDA actions	11
Warning letters	0
Recalls	11
Approval records	0
Form 483 inspection citations	0
Most recent action	June 24, 2026

Risk pattern analysis

Argus HQ analysis — not an FDA finding

This section is Argus HQ analysis, not an FDA finding. ConMed Corporation has 11 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 2026-06-24, Argus HQ recorded a FDA recall for ConMed Corporation, rated "high" severity in Argus HQ's classification: ConMed Corporation — Class II recall: ConMed AirSeal 8mm Access Port and Low Profile Obturator with Bladeless Optical… An FDA recall record reflects a firm removing or correcting a product already in distribution because it does not meet FDA requirements. On 2026-06-24, Argus HQ recorded a FDA recall for ConMed Corporation, rated "high" severity in Argus HQ's classification: ConMed Corporation — Class II recall: ConMed AirSeal 12mm Access Port and Obturator with Blunt Tip, 100mm Length. Cata… An FDA recall record reflects a firm removing or correcting a product already in distribution because it does not meet FDA requirements. On 2026-06-24, Argus HQ recorded a FDA recall for ConMed Corporation, rated "high" severity in Argus HQ's classification: ConMed Corporation — Class II recall: ConMed AirSeal 12mm Access Port and Palm Grip Obturator with Bladeless Optical T… An FDA recall record reflects a firm removing or correcting a product already in distribution because it does not meet FDA requirements. On 2026-06-24, Argus HQ recorded a FDA recall for ConMed Corporation, rated "high" severity in Argus HQ's classification: ConMed Corporation — Class II recall: ConMed AirSeal 12 mm Access Port and Obturator with Blunt Tip, 120mm Length. Cat… An FDA recall record reflects a firm removing or correcting a product already in distribution because it does not meet FDA requirements. On 2026-06-24, Argus HQ recorded a FDA recall for ConMed Corporation, rated "high" severity in Argus HQ's classification: ConMed Corporation — Class II recall: ConMed AirSeal 12mm Access Port and Palm Grip Obturator with Bladeless Optical T… An FDA recall record reflects a firm removing or correcting a product already in distribution because it does not meet FDA requirements. On 2026-06-24, Argus HQ recorded a FDA recall for ConMed Corporation, rated "high" severity in Argus HQ's classification: ConMed Corporation — Class II recall: ConMed AirSeal 5mm Access Port and Low Profile Obturator with Bladeless Optical… An FDA recall record reflects a firm removing or correcting a product already in distribution because it does not meet FDA requirements. On 2026-06-24, Argus HQ recorded a FDA recall for ConMed Corporation, rated "high" severity in Argus HQ's classification: ConMed Corporation — Class II recall: ConMed AirSeal 12mm Access Port and Low Profile Obturator with Bladeless Optical… An FDA recall record reflects a firm removing or correcting a product already in distribution because it does not meet FDA requirements. On 2026-06-24, Argus HQ recorded a FDA recall for ConMed Corporation, rated "high" severity in Argus HQ's classification: ConMed Corporation — Class II recall: ConMed AirSeal 5 mm Smooth Access Port and Obturator with Blunt Tip, 150mm Lengt… An FDA recall record reflects a firm removing or correcting a product already in distribution because it does not meet FDA requirements. On 2026-06-24, Argus HQ recorded a FDA recall for ConMed Corporation, rated "high" severity in Argus HQ's classification: ConMed Corporation — Class II recall: ConMed AirSeal 8mm Access Port and Low Profile Obturator with Bladeless Optical… An FDA recall record reflects a firm removing or correcting a product already in distribution because it does not meet FDA requirements. On 2026-06-24, Argus HQ recorded a FDA recall for ConMed Corporation.

Frequently asked questions

What is the most recent FDA action on file for ConMed Corporation?: June 24, 2026. Argus HQ ingests new FDA enforcement records daily.
Has ConMed Corporation had product recalls?: Yes, 11 recalls on file. See the full history below for each one.
Is this FDA enforcement data for ConMed Corporation 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 ConMed Corporation had?: Argus HQ has recorded 11 FDA events for ConMed Corporation: 0 warning letters, 11 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.

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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). FDA Actions Against ConMed Corporation. Digital Empire LLC. Retrieved from https://argushq.ai/company/conmed-corporation

MLA

"FDA Actions Against ConMed Corporation." Argus HQ Research, Digital Empire LLC, 2026, argushq.ai/company/conmed-corporation.

Chicago

Argus HQ Research. "FDA Actions Against ConMed Corporation." Digital Empire LLC. Accessed July 13, 2026. https://argushq.ai/company/conmed-corporation.

BibTeX

@misc{argushq_argushq_ai_company_conmed_corporation_2026,
  title = {FDA Actions Against ConMed Corporation},
  author = {{Argus HQ Research}},
  year = {2026},
  publisher = {Digital Empire LLC},
  url = {https://argushq.ai/company/conmed-corporation},
  note = {Accessed: July 13, 2026}
}

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