How many FDA actions has Oscor Inc. had?

Argus HQ has recorded 3 FDA events for Oscor Inc.: 0 warning letters, 3 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 Oscor Inc.?

The most recent FDA event Argus HQ has on file for Oscor Inc. is dated 2026-07-22, 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 Oscor 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 Oscor Inc. is observed, this page's event count and history update automatically.

How many FDA actions does Argus HQ track for Oscor Inc.?

3 total: 0 warning letters, 3 recalls, 0 approval records, and 0 Form 483 inspection citations.

Oscor Inc. — FDA Compliance Timeline

At a glance: Argus HQ has recorded 3 FDA events for Oscor Inc.: 0 warning letters, 3 recalls, 0 approvals, and 0 inspection 483 observations. These events span from 2026-07-22 to 2026-07-22. 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.

FDA action counts

Total FDA actions	3
Warning letters	0
Recalls	3
Approval records	0
Form 483 inspection citations	0
Most recent action	July 22, 2026

Risk pattern analysis

Argus HQ analysis — not an FDA finding

This section is Argus HQ analysis, not an FDA finding. Oscor Inc. has 3 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 2026-07-22, Argus HQ recorded an FDA recall for Oscor Inc., rated "critical" severity in Argus HQ's classification: Oscor Inc. — Class I recall: Abiomed REF: 0052-3006, Introducer Kit for Impella Hemostatic Peel Away Introd…. On 2026-07-22, Argus HQ recorded an FDA recall for Oscor Inc., rated "critical" severity in Argus HQ's classification: Oscor Inc. — Class I recall: Abiomed REF: 0052-3021, Introducer Kit for Impella Hemostatic Peel Away Introd…. On 2026-07-22, Argus HQ recorded an FDA recall for Oscor Inc., rated "critical" severity in Argus HQ's classification: Oscor Inc. — Class I recall: Abiomed REF: 0052-3025, Introducer Kit for Impella Hemostatic Peel Away Introd…. 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. 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.

Frequently asked questions

How many FDA actions has Oscor Inc. had?: Argus HQ has recorded 3 FDA events for Oscor Inc.: 0 warning letters, 3 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 Oscor Inc.?: The most recent FDA event Argus HQ has on file for Oscor Inc. is dated 2026-07-22, 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 Oscor 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 Oscor Inc. is observed, this page's event count and history update automatically.
How many FDA actions does Argus HQ track for Oscor Inc.?: 3 total: 0 warning letters, 3 recalls, 0 approval records, and 0 Form 483 inspection citations.

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

Verified from FDA.gov · Last updated: Jul 22, 2026

Cite this record

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

APA

Argus HQ Research (2026). Oscor Inc. — FDA Compliance Timeline. Digital Empire Holdings LLC. Retrieved from https://argushq.ai/company/oscor-inc

MLA

"Oscor Inc. — FDA Compliance Timeline." Argus HQ Research, Digital Empire Holdings LLC, 2026, argushq.ai/company/oscor-inc.

Chicago

Argus HQ Research. "Oscor Inc. — FDA Compliance Timeline." Digital Empire Holdings LLC. Accessed July 28, 2026. https://argushq.ai/company/oscor-inc.

BibTeX

@misc{argushq_argushq_ai_company_oscor_inc_2026,
  title = {Oscor Inc. — FDA Compliance Timeline},
  author = {{Argus HQ Research}},
  year = {2026},
  publisher = {Digital Empire Holdings LLC},
  url = {https://argushq.ai/company/oscor-inc},
  note = {Accessed: July 28, 2026}
}

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