Medline Probe Cover Kits Recall: Inadequate Barrier Risk in Ultrasound Gel

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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 Probe Cover Kits with Model Number DYNDA1219 because the probe covers may have an inadequate barrier at the seams. This could lead to contamination during ultrasound procedures, so affected users should stop using these kits immediately.

Why it’s dangerous

The probe covers may have an inadequate barrier at the seams, allowing contaminants to enter the ultrasound gel. This could lead to contamination during diagnostic procedures, potentially causing infections or other complications.

Who’s affected

Healthcare professionals using ultrasound equipment are most at risk. Patients receiving ultrasound procedures with these kits could be exposed to contamination.

How to tell if you have this one

Check for Model Number DYNDA1219 on the Probe Cover Pack. These kits were distributed by Medline between December 2017 and May 2023.

Brand
Medline
Category
Medical device

Based on the official FDA remedy

What to do — step by step

Stop Using Kits
Immediately stop using any Probe Cover Kits with Model Number DYNDA1219 as they may have an inadequate barrier at the seams.

✎ GovInfoNow

Questions people ask

What model number is affected?

Model Number DYNDA1219

When were these kits distributed?

From December 2017 to May 2023

How can I check if I have the affected product?

Look for Model Number DYNDA1219 on the Probe Cover Pack. These kits were distributed by Medline between December 2017 and May 2023.

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-2201-2023 — Medline Medline

Hello,

I own a Medline that is covered by recall Z-2201-2023 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.

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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-2201-2023 (May 18, 2023) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-2201-2023 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 Medline Probe Cover Kits containing sterile Ultrasound Gel, Labeled as the following: PROBE COVER PACK, Model Number

Use caution until it’s fixed