Has Medline Industries, LP had other FDA enforcement actions?

Yes. Argus HQ has recorded 293 total FDA actions tied to Medline Industries, LP: 0 warning letters, 293 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 2026-06-24; Argus observed and indexed it on 2026-07-09.

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

Medline Industries, LP — Class II recall: MEDLINE Medical Procedure Kits labeled as: 1) D AND C PACK, Medline Kit Numbe…

Name: FDA Recall Record — Medline Industries, LP
Creator: Argus HQ
Published: 2026-06-24
License: https://argushq.ai/methodology

Event date: 2026-06-24 00:00:00Z
Observed: 2026-07-09 22:52:04Z
Source ID: Z-2504-2026
Payload hash: bfb2164d9ac0eaedf5d80ca9…

Summary

During an internal review, Medline identified representative samples did not meet applicable performance specifications. Identified issues include irregularities in catheter surface finish, instances where the catheter connector detached prematurely from the catheter funnel, and limited cases where… Status: Ongoing.

Entities

Medline Industries, LP

View source record ↗

Frequently asked questions

Has Medline Industries, LP had other FDA enforcement actions?: Yes. Argus HQ has recorded 293 total FDA actions tied to Medline Industries, LP: 0 warning letters, 293 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 2026-06-24; Argus observed and indexed it on 2026-07-09.
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). Medline Industries, LP — Class II recall: MEDLINE Medical Procedure Kits labeled as:    1) D AND C PACK, Medline Kit Numbe…. Digital Empire Holdings LLC. Retrieved from https://argushq.ai/events/fda-recall-medline-industries-lp-z-2504-2026

MLA

"Medline Industries, LP — Class II recall: MEDLINE Medical Procedure Kits labeled as:    1) D AND C PACK, Medline Kit Numbe…." Argus HQ Research, Digital Empire Holdings LLC, 2026, argushq.ai/events/fda-recall-medline-industries-lp-z-2504-2026.

Chicago

Argus HQ Research. "Medline Industries, LP — Class II recall: MEDLINE Medical Procedure Kits labeled as:    1) D AND C PACK, Medline Kit Numbe…." Digital Empire Holdings LLC. Accessed August 27, 2026. https://argushq.ai/events/fda-recall-medline-industries-lp-z-2504-2026.

BibTeX

@misc{argushq_argushq_ai_events_fda_recall_medline_industries_lp_z_2504_2026_2026,
  title = {Medline Industries, LP — Class II recall: MEDLINE Medical Procedure Kits labeled as:    1) D AND C PACK, Medline Kit Numbe…},
  author = {{Argus HQ Research}},
  year = {2026},
  publisher = {Digital Empire Holdings LLC},
  url = {https://argushq.ai/events/fda-recall-medline-industries-lp-z-2504-2026},
  note = {Accessed: August 27, 2026}
}

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