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

Yes. Argus HQ has recorded 14 total FDA actions tied to Bard Access Systems, Inc.: 0 warning letters, 14 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 high severity by Argus HQ. FDA published the underlying record on 2026-07-08; Argus observed and indexed it on 2026-07-14.

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 · high

Bard Access Systems, Inc. — Class II recall: OTP5000 THORA/PARA TRAY, 5FR, NON-VALVED UDI-DI Code: 0110885403284748 PIG12…

Name: FDA Recall Record — Bard Access Systems, Inc.
Creator: Argus HQ
Published: 2026-07-08
License: https://argushq.ai/methodology

Event date: 2026-07-08 00:00:00Z
Observed: 2026-07-14 04:20:24Z
Source ID: Z-2655-2026
Payload hash: ca224689b9f55efaaa707eb1…

Summary

Due to lidocaine ampoules being manufactured under deficient manufacturing practices by manufacturer, lidocaine ampoules are currently being recalled by supplier. 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 14 total FDA actions tied to Bard Access Systems, Inc.: 0 warning letters, 14 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 high severity by Argus HQ. FDA published the underlying record on 2026-07-08; Argus observed and indexed it on 2026-07-14.
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 II recall: OTP5000	THORA/PARA TRAY, 5FR, NON-VALVED  UDI-DI Code: 0110885403284748    PIG12…. Digital Empire LLC. Retrieved from https://argushq.ai/events/fda-recall-bard-access-systems-inc-z-2655-2026

MLA

"Bard Access Systems, Inc. — Class II recall: OTP5000	THORA/PARA TRAY, 5FR, NON-VALVED  UDI-DI Code: 0110885403284748    PIG12…." Argus HQ Research, Digital Empire LLC, 2026, argushq.ai/events/fda-recall-bard-access-systems-inc-z-2655-2026.

Chicago

Argus HQ Research. "Bard Access Systems, Inc. — Class II recall: OTP5000	THORA/PARA TRAY, 5FR, NON-VALVED  UDI-DI Code: 0110885403284748    PIG12…." Digital Empire LLC. Accessed July 14, 2026. https://argushq.ai/events/fda-recall-bard-access-systems-inc-z-2655-2026.

BibTeX

@misc{argushq_argushq_ai_events_fda_recall_bard_access_systems_inc_z_2655_2026_2026,
  title = {Bard Access Systems, Inc. — Class II recall: OTP5000	THORA/PARA TRAY, 5FR, NON-VALVED  UDI-DI Code: 0110885403284748    PIG12…},
  author = {{Argus HQ Research}},
  year = {2026},
  publisher = {Digital Empire LLC},
  url = {https://argushq.ai/events/fda-recall-bard-access-systems-inc-z-2655-2026},
  note = {Accessed: July 14, 2026}
}

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