How many FDA actions has C.R. Bard Inc had?

Argus HQ has recorded 1 FDA events for C.R. Bard Inc: 0 warning letters, 1 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 C.R. Bard Inc?

The most recent FDA event Argus HQ has on file for C.R. Bard Inc is dated 2026-05-27, 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 C.R. Bard 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 C.R. Bard Inc is observed, this page's event count and history update automatically.

How many FDA actions does Argus HQ track for C.R. Bard Inc?

1 total: 0 warning letters, 1 recall, 0 approval records, and 0 Form 483 inspection citations.

FDA Enforcement History: C.R. Bard Inc

At a glance: Argus HQ has recorded 1 FDA events for C.R. Bard Inc: 0 warning letters, 1 recalls, 0 approvals, and 0 inspection 483 observations. These events span from 2026-05-27 to 2026-05-27. 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.

FDA action counts

Total FDA actions	1
Warning letters	0
Recalls	1
Approval records	0
Form 483 inspection citations	0
Most recent action	May 27, 2026

Enforcement history

On 2026-05-27, Argus HQ recorded an FDA recall for C.R. Bard Inc, rated "high" severity in Argus HQ's classification: C.R. Bard Inc — Class II recall: Silastic Foley Catheters Silastic Brand Foley Catheter 30cc REF: 33416 33418…. 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.

Risk pattern analysis

Argus HQ analysis — not an FDA finding

This section is Argus HQ analysis, not an FDA finding. C.R. Bard Inc 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.

Frequently asked questions

How many FDA actions has C.R. Bard Inc had?: Argus HQ has recorded 1 FDA events for C.R. Bard Inc: 0 warning letters, 1 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 C.R. Bard Inc?: The most recent FDA event Argus HQ has on file for C.R. Bard Inc is dated 2026-05-27, 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 C.R. Bard 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 C.R. Bard Inc is observed, this page's event count and history update automatically.
How many FDA actions does Argus HQ track for C.R. Bard Inc?: 1 total: 0 warning letters, 1 recall, 0 approval records, and 0 Form 483 inspection citations.

Every FDA action tied to this company, the week it happens.

Free weekly briefing. Real-time alerts on paid plans.

C.R. Bard Inc — Class II recall: Silastic Foley Catheters Silastic Brand Foley Catheter 30cc REF: 33416 33418… →

Compare with

Two different companies merged onto this page by mistake? Or a name variant missing? Tell us — corrections@argushq.ai

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 Enforcement History: C.R. Bard Inc. Digital Empire LLC. Retrieved from https://argushq.ai/company/c-r-bard-inc

MLA

"FDA Enforcement History: C.R. Bard Inc." Argus HQ Research, Digital Empire LLC, 2026, argushq.ai/company/c-r-bard-inc.

Chicago

Argus HQ Research. "FDA Enforcement History: C.R. Bard Inc." Digital Empire LLC. Accessed July 13, 2026. https://argushq.ai/company/c-r-bard-inc.

BibTeX

@misc{argushq_argushq_ai_company_c_r_bard_inc_2026,
  title = {FDA Enforcement History: C.R. Bard Inc},
  author = {{Argus HQ Research}},
  year = {2026},
  publisher = {Digital Empire LLC},
  url = {https://argushq.ai/company/c-r-bard-inc},
  note = {Accessed: July 13, 2026}
}

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