Does Argus HQ track new FDA actions for AVID Medical, 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 AVID Medical, Inc. is observed, this page's event count and history update automatically.

How many FDA actions does Argus HQ track for AVID Medical, Inc.?

14 total: 0 warning letters, 14 recalls, 0 approval records, and 0 Form 483 inspection citations.

What is the most recent FDA action on file for AVID Medical, Inc.?

June 17, 2026. Argus HQ ingests new FDA enforcement records daily.

Has AVID Medical, Inc. had product recalls?

Yes, 14 recalls on file. See the full history below for each one.

AVID Medical, Inc. — FDA Compliance Timeline

Here's the summary: Argus HQ has recorded 14 FDA events for AVID Medical, Inc.: 0 warning letters, 14 recalls, 0 approvals, and 0 inspection 483 observations. These events span from 2026-05-13 to 2026-06-17. 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.

FDA action counts

Total FDA actions	14
Warning letters	0
Recalls	14
Approval records	0
Form 483 inspection citations	0
Most recent action	June 17, 2026

Risk pattern analysis

Argus HQ analysis — not an FDA finding

This section is Argus HQ analysis, not an FDA finding. AVID Medical, Inc. has 14 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 2026-05-13, Argus HQ recorded a FDA recall for AVID Medical, Inc., rated "critical" severity in Argus HQ's classification: AVID Medical, Inc. — Class I recall: Halyard HEART CATH, SELF REGIONAL kit. Model Number: SELF131-05. An FDA recall record reflects a firm removing or correcting a product already in distribution because it does not meet FDA requirements. On 2026-05-13, Argus HQ recorded a FDA recall for AVID Medical, Inc., rated "critical" severity in Argus HQ's classification: AVID Medical, Inc. — Class I recall: Halyard CARDIAC CATH PACK SAN23CARDQ kit. Model Number: DRCC36. An FDA recall record reflects a firm removing or correcting a product already in distribution because it does not meet FDA requirements. On 2026-05-13, Argus HQ recorded a FDA recall for AVID Medical, Inc., rated "critical" severity in Argus HQ's classification: AVID Medical, Inc. — Class I recall: Halyard CARDIAC CATH PACK kit. Model Number: EAMC1000-05, WAFB208-02. An FDA recall record reflects a firm removing or correcting a product already in distribution because it does not meet FDA requirements. On 2026-05-13, Argus HQ recorded a FDA recall for AVID Medical, Inc., rated "critical" severity in Argus HQ's classification: AVID Medical, Inc. — Class I recall: Halyard PERC TRAY kit. Model Numbers: SLPC34-01, SLPC34-02. An FDA recall record reflects a firm removing or correcting a product already in distribution because it does not meet FDA requirements. On 2026-05-13, Argus HQ recorded a FDA recall for AVID Medical, Inc., rated "critical" severity in Argus HQ's classification: AVID Medical, Inc. — Class I recall: Halyard CARDIAC CATH TRAY SHANDS JAX kit. Model Number: SHND401-04, SHND401-05. An FDA recall record reflects a firm removing or correcting a product already in distribution because it does not meet FDA requirements. On 2026-05-13, Argus HQ recorded a FDA recall for AVID Medical, Inc., rated "critical" severity in Argus HQ's classification: AVID Medical, Inc. — Class I recall: Halyard CATH LAB kit. Model Number: SACL75-01. An FDA recall record reflects a firm removing or correcting a product already in distribution because it does not meet FDA requirements. On 2026-05-13, Argus HQ recorded a FDA recall for AVID Medical, Inc., rated "critical" severity in Argus HQ's classification: AVID Medical, Inc. — Class I recall: Halyard CATH LAB kit. Model Number: SACL75AM. An FDA recall record reflects a firm removing or correcting a product already in distribution because it does not meet FDA requirements. On 2026-05-13, Argus HQ recorded a FDA recall for AVID Medical, Inc., rated "critical" severity in Argus HQ's classification: AVID Medical, Inc. — Class I recall: Halyard NEURO IR PERIPHERAL (PS 64405) kit. Model Number: UINR44-01. An FDA recall record reflects a firm removing or correcting a product already in distribution because it does not meet FDA requirements. On 2026-05-13, Argus HQ recorded a FDA recall for AVID Medical, Inc., rated "critical" severity in Argus HQ's classification: AVID Medical, Inc. — Class I recall: Halyard SAMMC ANGIOGRAPHY kit. Model Numbers: SAMM066-15. An FDA recall record reflects a firm removing or correcting a product already in distribution because it does not meet FDA requirements. On 2026-05-13, Argus HQ recorded a FDA recall for AVID Medical, Inc., rated "critical" severity in Argus HQ's classification: AVID Medical, Inc. — Class I recall: Halyard VA DETROIT CATH LAB.

Frequently asked questions

Does Argus HQ track new FDA actions for AVID Medical, 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 AVID Medical, Inc. is observed, this page's event count and history update automatically.
How many FDA actions does Argus HQ track for AVID Medical, Inc.?: 14 total: 0 warning letters, 14 recalls, 0 approval records, and 0 Form 483 inspection citations.
What is the most recent FDA action on file for AVID Medical, Inc.?: June 17, 2026. Argus HQ ingests new FDA enforcement records daily.
Has AVID Medical, Inc. had product recalls?: Yes, 14 recalls on file. See the full history below for each one.

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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). AVID Medical, Inc. — FDA Compliance Timeline. Digital Empire LLC. Retrieved from https://argushq.ai/company/avid-medical-inc

MLA

"AVID Medical, Inc. — FDA Compliance Timeline." Argus HQ Research, Digital Empire LLC, 2026, argushq.ai/company/avid-medical-inc.

Chicago

Argus HQ Research. "AVID Medical, Inc. — FDA Compliance Timeline." Digital Empire LLC. Accessed July 13, 2026. https://argushq.ai/company/avid-medical-inc.

BibTeX

@misc{argushq_argushq_ai_company_avid_medical_inc_2026,
  title = {AVID Medical, Inc. — FDA Compliance Timeline},
  author = {{Argus HQ Research}},
  year = {2026},
  publisher = {Digital Empire LLC},
  url = {https://argushq.ai/company/avid-medical-inc},
  note = {Accessed: July 13, 2026}
}

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