Has Becton Dickinson Infusion Therapy Systems, Inc. had other FDA enforcement actions?

Yes. Argus HQ has recorded 13 total FDA actions tied to Becton Dickinson Infusion Therapy Systems, Inc.: 0 warning letters, 13 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 2025-07-02; Argus observed and indexed it on 2026-07-16.

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

Becton Dickinson Infusion Therapy Systems, Inc. — Class II recall: REF: 381423, BD Insyte Autoguard, Shielded IV Catheter, 22GA X 1.00 IN (0.9 X 25…

Name: FDA Recall Record — Becton Dickinson Infusion Therapy Systems, Inc.
Creator: Argus HQ
Published: 2025-07-02
License: https://argushq.ai/methodology

Event date: 2025-07-02 00:00:00Z
Observed: 2026-07-16 23:20:09Z
Source ID: Z-1999-2025
Payload hash: 20007bd3e817c71fa95b6524…

Summary

Due to customer complaints, there is the possibility that catheter needle may be slow to retract or fail to retract. Status: Ongoing.

Entities

Becton Dickinson Infusion Therapy Systems, Inc.

View source record ↗

Frequently asked questions

Has Becton Dickinson Infusion Therapy Systems, Inc. had other FDA enforcement actions?: Yes. Argus HQ has recorded 13 total FDA actions tied to Becton Dickinson Infusion Therapy Systems, Inc.: 0 warning letters, 13 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 2025-07-02; Argus observed and indexed it on 2026-07-16.
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 (2025). Becton Dickinson Infusion Therapy Systems, Inc. — Class II recall: REF: 381423, BD Insyte Autoguard, Shielded IV Catheter, 22GA X 1.00 IN (0.9 X 25…. Digital Empire Holdings LLC. Retrieved from https://argushq.ai/events/fda-recall-becton-dickinson-infusion-therapy-systems-inc-z-1999-2025

MLA

"Becton Dickinson Infusion Therapy Systems, Inc. — Class II recall: REF: 381423, BD Insyte Autoguard, Shielded IV Catheter, 22GA X 1.00 IN (0.9 X 25…." Argus HQ Research, Digital Empire Holdings LLC, 2025, argushq.ai/events/fda-recall-becton-dickinson-infusion-therapy-systems-inc-z-1999-2025.

Chicago

Argus HQ Research. "Becton Dickinson Infusion Therapy Systems, Inc. — Class II recall: REF: 381423, BD Insyte Autoguard, Shielded IV Catheter, 22GA X 1.00 IN (0.9 X 25…." Digital Empire Holdings LLC. Accessed July 23, 2026. https://argushq.ai/events/fda-recall-becton-dickinson-infusion-therapy-systems-inc-z-1999-2025.

BibTeX

@misc{argushq_argushq_ai_events_fda_recall_becton_dickinson_infusion_therapy_systems_inc_z_1999_2025_2025,
  title = {Becton Dickinson Infusion Therapy Systems, Inc. — Class II recall: REF: 381423, BD Insyte Autoguard, Shielded IV Catheter, 22GA X 1.00 IN (0.9 X 25…},
  author = {{Argus HQ Research}},
  year = {2025},
  publisher = {Digital Empire Holdings LLC},
  url = {https://argushq.ai/events/fda-recall-becton-dickinson-infusion-therapy-systems-inc-z-1999-2025},
  note = {Accessed: July 23, 2026}
}

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