Has Medline Industries, LP had other FDA enforcement actions?

Yes. Argus HQ has recorded 269 total FDA actions tied to Medline Industries, LP: 0 warning letters, 269 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 critical severity by Argus HQ. FDA published the underlying record on 2026-07-01; 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 · critical

Medline Industries, LP — Class I recall: Medline Convenience Kits: 1) DRAWER 6 CENTRAL LINE INSERTIO, Model Number: ACC…

Name: FDA Recall Record — Medline Industries, LP
Creator: Argus HQ
Published: 2026-07-01
License: https://argushq.ai/methodology

Event date: 2026-07-01 00:00:00Z
Observed: 2026-07-09 22:51:55Z
Source ID: Z-2454-2026
Payload hash: df94bbd74a08ffa0556edc1a…

Summary

The Medline Convenience Kits contain Arrow Kits and Sets that include Lidocaine Hydrochloride Injection, USP and Bupivacaine Hydrochloride in Dextrose Injection, USP which were recalled due to quality issues identified during a recent FDA inspection of the supplier. 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 269 total FDA actions tied to Medline Industries, LP: 0 warning letters, 269 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 critical severity by Argus HQ. FDA published the underlying record on 2026-07-01; 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 I recall: Medline Convenience Kits:   1) DRAWER 6 CENTRAL LINE INSERTIO, Model Number: ACC…. Digital Empire Holdings LLC. Retrieved from https://argushq.ai/events/fda-recall-medline-industries-lp-z-2454-2026

MLA

"Medline Industries, LP — Class I recall: Medline Convenience Kits:   1) DRAWER 6 CENTRAL LINE INSERTIO, Model Number: ACC…." Argus HQ Research, Digital Empire Holdings LLC, 2026, argushq.ai/events/fda-recall-medline-industries-lp-z-2454-2026.

Chicago

Argus HQ Research. "Medline Industries, LP — Class I recall: Medline Convenience Kits:   1) DRAWER 6 CENTRAL LINE INSERTIO, Model Number: ACC…." Digital Empire Holdings LLC. Accessed July 23, 2026. https://argushq.ai/events/fda-recall-medline-industries-lp-z-2454-2026.

BibTeX

@misc{argushq_argushq_ai_events_fda_recall_medline_industries_lp_z_2454_2026_2026,
  title = {Medline Industries, LP — Class I recall: Medline Convenience Kits:   1) DRAWER 6 CENTRAL LINE INSERTIO, Model Number: ACC…},
  author = {{Argus HQ Research}},
  year = {2026},
  publisher = {Digital Empire Holdings LLC},
  url = {https://argushq.ai/events/fda-recall-medline-industries-lp-z-2454-2026},
  note = {Accessed: July 23, 2026}
}

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