Has Bard Access Systems, Inc. had other FDA enforcement actions?

Yes. Argus HQ has recorded 15 total FDA actions tied to Bard Access Systems, Inc.: 0 warning letters, 15 recalls, 0 approval records, and 0 Form 483 inspection citations.

What kind of FDA record is this?

This is an Argus HQ record of a FDA Recall, tagged critical severity by Argus HQ. FDA published the underlying record on 2026-08-26; Argus observed and indexed it on 2026-09-08.

Where can I verify this record directly with FDA?

The verbatim FDA source record is the source of truth — Argus HQ links directly to it below. Always confirm against fda.gov before acting.

.hq

fda_recall · device_recall · critical

Bard Access Systems, Inc. — Class I recall: BD Needle Kit for Powered Driver 15mm x 15Ga, REF: D015151NK, BD Needle Kit for…

Name: FDA Recall Record — Bard Access Systems, Inc.
Creator: Argus HQ
Published: 2026-08-26
License: https://argushq.ai/methodology

Event date: 2026-08-26 00:00:00Z
Observed: 2026-09-08 04:20:32Z
Source ID: Z-2872-2026
Payload hash: 0ff10710d152cf216ed7dcd9…

Summary

After placement of intraosseous (IO) needle sets, used when intravenous access is difficult or impossible to obtain in emergent, urgent, or medically necessary cases, users may experience difficulty/inability to remove obturator, due to it locking to the needle hub, due to out-of-tolerance dimension… Status: Ongoing.

Entities

Bard Access Systems, Inc.

View source record ↗

Frequently asked questions

Has Bard Access Systems, Inc. had other FDA enforcement actions?: Yes. Argus HQ has recorded 15 total FDA actions tied to Bard Access Systems, Inc.: 0 warning letters, 15 recalls, 0 approval records, and 0 Form 483 inspection citations.
What kind of FDA record is this?: This is an Argus HQ record of a FDA Recall, tagged critical severity by Argus HQ. FDA published the underlying record on 2026-08-26; Argus observed and indexed it on 2026-09-08.
Where can I verify this record directly with FDA?: The verbatim FDA source record is the source of truth — Argus HQ links directly to it below. Always confirm against fda.gov before acting.

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). Bard Access Systems, Inc. — Class I recall: BD Needle Kit for Powered Driver 15mm x 15Ga, REF: D015151NK,  BD Needle Kit for…. Digital Empire Holdings LLC. Retrieved from https://argushq.ai/events/fda-recall-bard-access-systems-inc-z-2872-2026

MLA

"Bard Access Systems, Inc. — Class I recall: BD Needle Kit for Powered Driver 15mm x 15Ga, REF: D015151NK,  BD Needle Kit for…." Argus HQ Research, Digital Empire Holdings LLC, 2026, argushq.ai/events/fda-recall-bard-access-systems-inc-z-2872-2026.

Chicago

Argus HQ Research. "Bard Access Systems, Inc. — Class I recall: BD Needle Kit for Powered Driver 15mm x 15Ga, REF: D015151NK,  BD Needle Kit for…." Digital Empire Holdings LLC. Accessed September 8, 2026. https://argushq.ai/events/fda-recall-bard-access-systems-inc-z-2872-2026.

BibTeX

@misc{argushq_argushq_ai_events_fda_recall_bard_access_systems_inc_z_2872_2026_2026,
  title = {Bard Access Systems, Inc. — Class I recall: BD Needle Kit for Powered Driver 15mm x 15Ga, REF: D015151NK,  BD Needle Kit for…},
  author = {{Argus HQ Research}},
  year = {2026},
  publisher = {Digital Empire Holdings LLC},
  url = {https://argushq.ai/events/fda-recall-bard-access-systems-inc-z-2872-2026},
  note = {Accessed: September 8, 2026}
}

Informational only. Not legal, financial, or medical advice.