Medline Custom Sterile Procedural Kits: Sterility Risk in Ultrasound Gel

Take action

Contact the company & request your remedy

Recalling firmMEDLINE INDUSTRIES, LP - Northfield3 Lakes Dr, N/A · Northfield, IL 60093-2753

No email on file — write to the address above instead.

✎ GovInfoNow plain-language explainer

What happened, in plain English

Medline is recalling custom sterile and non-sterile procedural kits that contain Turkuaz ultrasound gel. The gel may not meet sterility standards, which could lead to infections during medical procedures.

Why it’s dangerous

The ultrasound gel in the kits may not meet sterility requirements. This could allow bacteria to enter the body during medical procedures, increasing infection risk.

Who’s affected

Healthcare professionals using these kits for medical procedures are most at risk. Patients receiving procedures with these kits could face infection risks.

How to tell if you have this one

Check for model numbers DYNJ58351A (CATH LAB PACK) or DYNJ63341B (PV CAROTID PACK) on the kit. These kits were sold by Medline between April 2020 and April 2023.

Brand
Medline
Category
Medical device

Based on the official FDA remedy

What to do — step by step

Check Model Numbers
Look for model numbers DYNJ58351A or DYNJ63341B on the kit label.

✎ GovInfoNow

Questions people ask

What model numbers are affected?

Model numbers DYNJ58351A (CATH LAB PACK) and DYNJ63341B (PV CAROTID PACK).

When were these kits sold?

Sold by Medline between April 2020 and April 2023.

Is there a remedy for this recall?

The recall record does not specify a remedy.

Take action

Contact Medline

We’ve drafted a message you can send Medline to request your refund or repair — edit it as you like.

✉️ Open in email

Subject: Recall Z-2337-2023 — Medline Medline

Hello,

I own a Medline that is covered by recall Z-2337-2023 from Medline.

I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this?

Thank you.

Similar recalls

From people who’ve dealt with this

Experiences, tips, and questions from readers. Every comment is reviewed before it appears.

No comments yet — be the first to share your experience.

Where this comes from

The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.

Official source: FDA Recall #Z-2337-2023 (May 15, 2023) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-2337-2023 to see it in context.
Plain-language summary written by qwen3:4b on August 19, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.

MEDLINE INDUSTRIES, LP - Northfield recalls Custom Sterile and Non-Sterile Procedural Kits containing Turkuaz Ultrasound Gel. Labeled as the following: a. CATH LAB

Lower-risk recall