Has BD SWITZERLAND SARL had other FDA enforcement actions?

Yes. Argus HQ has recorded 4 total FDA actions tied to BD SWITZERLAND SARL: 0 warning letters, 4 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 2026-08-19; Argus observed and indexed it on 2026-08-26.

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

BD SWITZERLAND SARL — Class II recall: 60 In Non-DEHP Minibore Extension Set RES ME2010 UDI-DI code: 10885403236235…

Name: FDA Recall Record — BD SWITZERLAND SARL
Creator: Argus HQ
Published: 2026-08-19
License: https://argushq.ai/methodology

Event date: 2026-08-19 00:00:00Z
Observed: 2026-08-26 04:20:39Z
Source ID: Z-2941-2026
Payload hash: 5a728ec362788084bee0919f…

Summary

Products may not have received adequate sterilization processing. Status: Ongoing.

Entities

BD SWITZERLAND SARL

View source record ↗

Frequently asked questions

Has BD SWITZERLAND SARL had other FDA enforcement actions?: Yes. Argus HQ has recorded 4 total FDA actions tied to BD SWITZERLAND SARL: 0 warning letters, 4 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 2026-08-19; Argus observed and indexed it on 2026-08-26.
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). BD SWITZERLAND SARL — Class II recall: 60 In Non-DEHP Minibore Extension Set RES ME2010  UDI-DI code: 10885403236235…. Digital Empire Holdings LLC. Retrieved from https://argushq.ai/events/fda-recall-bd-switzerland-sarl-z-2941-2026

MLA

"BD SWITZERLAND SARL — Class II recall: 60 In Non-DEHP Minibore Extension Set RES ME2010  UDI-DI code: 10885403236235…." Argus HQ Research, Digital Empire Holdings LLC, 2026, argushq.ai/events/fda-recall-bd-switzerland-sarl-z-2941-2026.

Chicago

Argus HQ Research. "BD SWITZERLAND SARL — Class II recall: 60 In Non-DEHP Minibore Extension Set RES ME2010  UDI-DI code: 10885403236235…." Digital Empire Holdings LLC. Accessed September 29, 2026. https://argushq.ai/events/fda-recall-bd-switzerland-sarl-z-2941-2026.

BibTeX

@misc{argushq_argushq_ai_events_fda_recall_bd_switzerland_sarl_z_2941_2026_2026,
  title = {BD SWITZERLAND SARL — Class II recall: 60 In Non-DEHP Minibore Extension Set RES ME2010  UDI-DI code: 10885403236235…},
  author = {{Argus HQ Research}},
  year = {2026},
  publisher = {Digital Empire Holdings LLC},
  url = {https://argushq.ai/events/fda-recall-bd-switzerland-sarl-z-2941-2026},
  note = {Accessed: September 29, 2026}
}

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