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

How many FDA actions does Argus HQ track for Bard Access Systems, 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 Bard Access Systems, Inc.?

July 8, 2026. Argus HQ ingests new FDA enforcement records daily.

Has Bard Access Systems, Inc. had product recalls?

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

Bard Access Systems, Inc. — FDA Enforcement History

FDA action counts

Total FDA actions	14
Warning letters	0
Recalls	14
Approval records	0
Form 483 inspection citations	0
Most recent action	July 8, 2026

The short version: Argus HQ has recorded 14 FDA events for Bard Access Systems, Inc.: 0 warning letters, 14 recalls, 0 approvals, and 0 inspection 483 observations. These events span from 2026-07-08 to 2026-07-08. 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. Bard Access Systems, 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. Argus HQ ingests these records directly from FDA's own public enforcement and approval databases rather than from company disclosures.

Enforcement history

On 2026-07-08, Argus HQ recorded an FDA recall for Bard Access Systems, Inc., rated "high" severity in Argus HQ's classification: Bard Access Systems, Inc. — Class II recall: CK000495A Poly Midline Catheter 4 Fr Single-Lumen UDI-DI Code: 00801741121609…. On 2026-07-08, Argus HQ recorded an FDA recall for Bard Access Systems, Inc., rated "high" severity in Argus HQ's classification: Bard Access Systems, Inc. — Class II recall: CK000980A PowerMidline Catheter 4 Fr Dual-Lumen UDI-DI Code: 00801741236150…. On 2026-07-08, Argus HQ recorded an FDA recall for Bard Access Systems, Inc., rated "high" severity in Argus HQ's classification: Bard Access Systems, Inc. — Class II recall: 5625240 DuoGlide Short-Term Straight Dialysis Catheter 13 Fr Dual-Lumen UDI-DI…. On 2026-07-08, Argus HQ recorded an FDA recall for Bard Access Systems, Inc., rated "high" severity in Argus HQ's classification: Bard Access Systems, Inc. — Class II recall: 5605150 Power-Trialysis Short-Term Straight Dialysis Catheter 13 Fr Triple-Lumen…. On 2026-07-08, Argus HQ recorded an FDA recall for Bard Access Systems, Inc., rated "high" severity in Argus HQ's classification: Bard Access Systems, Inc. — Class II recall: CK000525B PowerPICC Provena SOLO Catheter 4 Fr Dual-Lumen UDI-DI Code: 00801741…. On 2026-07-08, Argus HQ recorded an FDA recall for Bard Access Systems, Inc., rated "high" severity in Argus HQ's classification: Bard Access Systems, Inc. — Class II recall: 1174108 PowerPICC Catheter 4 Fr Single-Lumen UDI-DI Code: 00801741154935 129…. On 2026-07-08, Argus HQ recorded an FDA recall for Bard Access Systems, Inc., rated "high" severity in Argus HQ's classification: Bard Access Systems, Inc. — Class II recall: 5855240 Power-Trialysis Slim-Cath Straight Short-Term Dialysis Catheter 12 Fr Tr…. On 2026-07-08, Argus HQ recorded an FDA recall for Bard Access Systems, Inc., rated "high" severity in Argus HQ's classification: Bard Access Systems, Inc. — Class II recall: 7617408 Groshong NXT ClearVue Catheter 4 Fr Single-Lumen UDI-DI Code: 008017410…. On 2026-07-08, Argus HQ recorded an FDA recall for Bard Access Systems, Inc., rated "high" severity in Argus HQ's classification: Bard Access Systems, Inc. — Class II recall: CK000880 Provena Midline Catheter 4 Fr Dual-Lumen UDI-DI Code: 00801741188770…. On 2026-07-08, Argus HQ recorded an FDA recall for Bard Access Systems, Inc., rated "high" severity in Argus HQ's classification: Bard Access Systems, Inc. — Class II recall: CK000662 PowerPICC SOLO HF Catheter 5 Fr Triple-Lumen UDI-DI Code: 00801741129…. On 2026-07-08, Argus HQ recorded an FDA recall for Bard Access Systems, Inc., rated "high" severity in Argus HQ's classification: Bard Access Systems, Inc. — Class II recall: CK000727 PowerMidline Catheter 4 Fr Single-Lumen UDI-DI Code: 00801741138478…. On 2026-07-08, Argus HQ recorded an FDA recall for Bard Access Systems, Inc., rated "high" severity in Argus HQ's classification: Bard Access Systems, Inc. — Class II recall: 1274108D PowerPICC SV Catheter 4 Fr Dual-Lumen REKW2449 00801741087110 3173108D….

Frequently asked questions

Does Argus HQ track new FDA actions for Bard Access Systems, 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 Bard Access Systems, Inc. is observed, this page's event count and history update automatically.
How many FDA actions does Argus HQ track for Bard Access Systems, 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 Bard Access Systems, Inc.?: July 8, 2026. Argus HQ ingests new FDA enforcement records daily.
Has Bard Access Systems, 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

Verified from FDA.gov · Last updated: Jul 8, 2026

Cite this record

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

APA

Argus HQ Research (2026). Bard Access Systems, Inc. — FDA Enforcement History. Digital Empire Holdings LLC. Retrieved from https://argushq.ai/company/bard-access-systems-inc

MLA

"Bard Access Systems, Inc. — FDA Enforcement History." Argus HQ Research, Digital Empire Holdings LLC, 2026, argushq.ai/company/bard-access-systems-inc.

Chicago

Argus HQ Research. "Bard Access Systems, Inc. — FDA Enforcement History." Digital Empire Holdings LLC. Accessed August 28, 2026. https://argushq.ai/company/bard-access-systems-inc.

BibTeX

@misc{argushq_argushq_ai_company_bard_access_systems_inc_2026,
  title = {Bard Access Systems, Inc. — FDA Enforcement History},
  author = {{Argus HQ Research}},
  year = {2026},
  publisher = {Digital Empire Holdings LLC},
  url = {https://argushq.ai/company/bard-access-systems-inc},
  note = {Accessed: August 28, 2026}
}

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