Medline recalls probe cover kits for ultrasound procedures due to potential inadequate seam barriers. Affected kits include fetal surgery and ablation models sold from Dec 2017 to May 2023. Contact Medline for details.
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 the covers may have weak seams that don't protect against contamination. This could lead to infection risks during medical procedures if the covers are used improperly.
The probe covers may have weak seams that don't properly seal, potentially allowing contaminants to enter the ultrasound gel. This could increase infection risk during procedures if the covers are not used correctly.
Healthcare providers using Medline probe cover kits for ultrasound procedures, especially those with the specific model numbers listed in the recall. The risk is low for most users as the covers are designed for single-use and the hazard is not severe.
Check for model numbers CDS840214P (fetal surgery) or DYNJ82725 (ablation) on the kit packaging. These kits were sold by Medline between December 2017 and May 2023.
Look for model numbers CDS840214P or DYNJ82725 on the probe cover kit packaging.
Reach out to Medline directly for instructions on how to return or replace the kit if it is affected.
The recall states the covers may have inadequate seam barriers, so they are not recommended for use until the recall is addressed.
Check for model numbers CDS840214P (fetal surgery) or DYNJ82725 (ablation) on the kit packaging. These kits were sold by Medline between December 2017 and May 2023.
The recall does not specify an immediate stop-use requirement, but affected kits should be contacted for return or replacement.
We’ve drafted a message you can send Medline to request your refund or repair — edit it as you like.
Subject: Recall Z-2189-2023 — Medline Medline Hello, I own a Medline that is covered by recall Z-2189-2023 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.
