Has Covidien LLC had other FDA enforcement actions?

Yes. Argus HQ has recorded 5 total FDA actions tied to Covidien LLC: 0 warning letters, 5 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

Covidien LLC — Class II recall: Covidien Shiley Disposable Decannulation Plug REF DDCP UDI-DI code: 108845220…

Name: FDA Recall Record — Covidien LLC
Creator: Argus HQ
Published: 2026-07-08
License: https://argushq.ai/methodology

Event date: 2026-07-08 00:00:00Z
Observed: 2026-07-14 04:20:22Z
Source ID: Z-2653-2026
Payload hash: 1b902c4c1909cbba34bd5c75…

Summary

Due to product labeling incorrectly including the symbol indicating non-DEHP (Bis(2-ethylhexyl) phthalate as the product includes 30 to 35% DEHP. Status: Ongoing.

Entities

Covidien LLC

View source record ↗

Frequently asked questions

Has Covidien LLC had other FDA enforcement actions?: Yes. Argus HQ has recorded 5 total FDA actions tied to Covidien LLC: 0 warning letters, 5 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). Covidien LLC — Class II recall: Covidien Shiley Disposable Decannulation Plug  REF  DDCP  UDI-DI code: 108845220…. Digital Empire LLC. Retrieved from https://argushq.ai/events/fda-recall-covidien-llc-z-2653-2026

MLA

"Covidien LLC — Class II recall: Covidien Shiley Disposable Decannulation Plug  REF  DDCP  UDI-DI code: 108845220…." Argus HQ Research, Digital Empire LLC, 2026, argushq.ai/events/fda-recall-covidien-llc-z-2653-2026.

Chicago

Argus HQ Research. "Covidien LLC — Class II recall: Covidien Shiley Disposable Decannulation Plug  REF  DDCP  UDI-DI code: 108845220…." Digital Empire LLC. Accessed July 14, 2026. https://argushq.ai/events/fda-recall-covidien-llc-z-2653-2026.

BibTeX

@misc{argushq_argushq_ai_events_fda_recall_covidien_llc_z_2653_2026_2026,
  title = {Covidien LLC — Class II recall: Covidien Shiley Disposable Decannulation Plug  REF  DDCP  UDI-DI code: 108845220…},
  author = {{Argus HQ Research}},
  year = {2026},
  publisher = {Digital Empire LLC},
  url = {https://argushq.ai/events/fda-recall-covidien-llc-z-2653-2026},
  note = {Accessed: July 14, 2026}
}

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