Medline recalls probe cover kits for ultrasound procedures due to potential inadequate barrier at seams. These kits may allow contaminants to enter during procedures. Affected models sold from Dec 2017 to May 2023.
Probe covers for use during diagnostic ultrasound procedures may have an inadequate barrier at the seams.
Medline is recalling probe cover kits used in ultrasound procedures because they may have weak seams that let contaminants enter. This could lead to infections or other complications during medical procedures. If you have any of the listed models, you should stop using them immediately.
The probe covers may have weak seams that do not properly seal, allowing contaminants to enter the ultrasound gel during procedures. This could lead to infections or other complications for patients and healthcare workers.
Healthcare professionals using these kits for ultrasound procedures are most at risk. Patients undergoing procedures with these kits could be exposed to contaminants.
Check for model numbers listed in the recall: DYNJ0429121G through DYNJ906086A and SPEC0232. These kits were sold between December 2017 and May 2023.
Discontinue use of any Medline probe cover kits with the listed model numbers as they may have inadequate seam barriers.
The recall states these kits may have inadequate barriers at the seams, so they are not safe to use without replacement.
You should stop using them immediately and contact Medline for a replacement or refund.
Check the model number on your kit against the list provided in the recall, which includes model numbers from DYNJ0429121G to DYNJ906086A and SPEC0232.
We’ve drafted a message you can send Medline to request your refund or repair — edit it as you like.
Subject: Recall Z-2186-2023 — Medline Medline Hello, I own a Medline that is covered by recall Z-2186-2023 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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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.
