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 2023-10-11; 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: 386862, BD Cathena Safety IV catheter with BD Multiguard Technology, 20 GA…

Name: FDA Recall Record — Becton Dickinson Infusion Therapy Systems, Inc.
Creator: Argus HQ
Published: 2023-10-11
License: https://argushq.ai/methodology

Event date: 2023-10-11 00:00:00Z
Observed: 2026-07-16 23:20:09Z
Source ID: Z-0025-2024
Payload hash: fb56e1b134fa9984a8019a04…

Summary

There is the potential that the safety shield may not properly engage on IV catheters. The needle can pull through the safety shield and disconnect from the needle safety shield leaving the contaminated needle point exposed. 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 2023-10-11; 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 (2023). Becton Dickinson Infusion Therapy Systems Inc. — Class II recall: REF: 386862, BD Cathena Safety IV catheter with BD Multiguard Technology, 20 GA…. Digital Empire LLC. Retrieved from https://argushq.ai/events/fda-recall-becton-dickinson-infusion-therapy-systems-inc-z-0025-2024

MLA

"Becton Dickinson Infusion Therapy Systems Inc. — Class II recall: REF: 386862, BD Cathena Safety IV catheter with BD Multiguard Technology, 20 GA…." Argus HQ Research, Digital Empire LLC, 2023, argushq.ai/events/fda-recall-becton-dickinson-infusion-therapy-systems-inc-z-0025-2024.

Chicago

Argus HQ Research. "Becton Dickinson Infusion Therapy Systems Inc. — Class II recall: REF: 386862, BD Cathena Safety IV catheter with BD Multiguard Technology, 20 GA…." Digital Empire LLC. Accessed July 17, 2026. https://argushq.ai/events/fda-recall-becton-dickinson-infusion-therapy-systems-inc-z-0025-2024.

BibTeX

@misc{argushq_argushq_ai_events_fda_recall_becton_dickinson_infusion_therapy_systems_inc_z_0025_2024_2023,
  title = {Becton Dickinson Infusion Therapy Systems Inc. — Class II recall: REF: 386862, BD Cathena Safety IV catheter with BD Multiguard Technology, 20 GA…},
  author = {{Argus HQ Research}},
  year = {2023},
  publisher = {Digital Empire LLC},
  url = {https://argushq.ai/events/fda-recall-becton-dickinson-infusion-therapy-systems-inc-z-0025-2024},
  note = {Accessed: July 17, 2026}
}

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