Has Medline Industries, LP had other FDA enforcement actions?

Yes. Argus HQ has recorded 266 total FDA actions tied to Medline Industries, LP: 0 warning letters, 266 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 2026-07-08; 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 · critical

Medline Industries, LP — Class I recall: Reprocessed Electrophysiology Catheters and Ultrasound Catheters Item no. 401…

Name: FDA Recall Record — Medline Industries, LP
Creator: Argus HQ
Published: 2026-07-08
License: https://argushq.ai/methodology

Event date: 2026-07-08 00:00:00Z
Observed: 2026-07-14 04:20:25Z
Source ID: Z-2615-2026
Payload hash: dcb563052af2ead058e6b331…

Summary

Expansion of RES 98277. Specific lots of reprocessed catheters may contain small particles of residual material. If devices with residual particulates on patient-contacting surfaces are used, there is a potential risk of an inflammatory response or systemic infection. If particulate were to dislodge… 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 266 total FDA actions tied to Medline Industries, LP: 0 warning letters, 266 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 2026-07-08; 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). Medline Industries, LP — Class I recall: Reprocessed Electrophysiology Catheters and Ultrasound Catheters    Item no. 401…. Digital Empire LLC. Retrieved from https://argushq.ai/events/fda-recall-medline-industries-lp-z-2615-2026

MLA

"Medline Industries, LP — Class I recall: Reprocessed Electrophysiology Catheters and Ultrasound Catheters    Item no. 401…." Argus HQ Research, Digital Empire LLC, 2026, argushq.ai/events/fda-recall-medline-industries-lp-z-2615-2026.

Chicago

Argus HQ Research. "Medline Industries, LP — Class I recall: Reprocessed Electrophysiology Catheters and Ultrasound Catheters    Item no. 401…." Digital Empire LLC. Accessed July 14, 2026. https://argushq.ai/events/fda-recall-medline-industries-lp-z-2615-2026.

BibTeX

@misc{argushq_argushq_ai_events_fda_recall_medline_industries_lp_z_2615_2026_2026,
  title = {Medline Industries, LP — Class I recall: Reprocessed Electrophysiology Catheters and Ultrasound Catheters    Item no. 401…},
  author = {{Argus HQ Research}},
  year = {2026},
  publisher = {Digital Empire LLC},
  url = {https://argushq.ai/events/fda-recall-medline-industries-lp-z-2615-2026},
  note = {Accessed: July 14, 2026}
}

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