What is the most recent FDA action against Bausch and Lomb Incorporated?

The most recent FDA event Argus HQ has on file for Bausch and Lomb Incorporated is dated 2026-03-20, 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 Bausch and Lomb Incorporated 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 Bausch and Lomb Incorporated is observed, this page's event count and history update automatically.

How many FDA actions does Argus HQ track for Bausch and Lomb Incorporated?

1 total: 0 warning letters, 0 recalls, 0 approval records, and 1 Form 483 inspection citation.

What is the most recent FDA action on file for Bausch and Lomb Incorporated?

March 20, 2026. Argus HQ ingests new FDA enforcement records daily.

Bausch and Lomb Incorporated — FDA Enforcement History

FDA action counts

Total FDA actions	1
Warning letters	0
Recalls	0
Approval records	0
Form 483 inspection citations	1
Most recent action	March 20, 2026

Key takeaway: Argus HQ has recorded 1 FDA events for Bausch and Lomb Incorporated: 0 warning letters, 0 recalls, 0 approvals, and 1 inspection 483 observations. These events span from 2026-03-20 to 2026-03-20. 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. 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. Bausch and Lomb Incorporated has 1 FDA event on file. 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 2026-03-20, Argus HQ recorded an FDA Form 483 inspection citation for Bausch and Lomb Incorporated, rated "high" severity in Argus HQ's classification: Bausch and Lomb Incorporated -- FDA 483: 1 observation (2026-03-20). 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

What is the most recent FDA action against Bausch and Lomb Incorporated?: The most recent FDA event Argus HQ has on file for Bausch and Lomb Incorporated is dated 2026-03-20, 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 Bausch and Lomb Incorporated 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 Bausch and Lomb Incorporated is observed, this page's event count and history update automatically.
How many FDA actions does Argus HQ track for Bausch and Lomb Incorporated?: 1 total: 0 warning letters, 0 recalls, 0 approval records, and 1 Form 483 inspection citation.
What is the most recent FDA action on file for Bausch and Lomb Incorporated?: March 20, 2026. Argus HQ ingests new FDA enforcement records daily.

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Bausch and Lomb Incorporated -- FDA 483: 1 observation (2026-03-20) →

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

Verified from FDA.gov · Last updated: Mar 20, 2026

Cite this record

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

APA

Argus HQ Research (2026). Bausch and Lomb Incorporated — FDA Enforcement History. Digital Empire Holdings LLC. Retrieved from https://argushq.ai/company/bausch-and-lomb-incorporated

MLA

"Bausch and Lomb Incorporated — FDA Enforcement History." Argus HQ Research, Digital Empire Holdings LLC, 2026, argushq.ai/company/bausch-and-lomb-incorporated.

Chicago

Argus HQ Research. "Bausch and Lomb Incorporated — FDA Enforcement History." Digital Empire Holdings LLC. Accessed August 17, 2026. https://argushq.ai/company/bausch-and-lomb-incorporated.

BibTeX

@misc{argushq_argushq_ai_company_bausch_and_lomb_incorporated_2026,
  title = {Bausch and Lomb Incorporated — FDA Enforcement History},
  author = {{Argus HQ Research}},
  year = {2026},
  publisher = {Digital Empire Holdings LLC},
  url = {https://argushq.ai/company/bausch-and-lomb-incorporated},
  note = {Accessed: August 17, 2026}
}

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