Medline recalls 100+ probe cover kits for ultrasound procedures due to potential inadequate seam barriers. These kits may allow contamination during procedures. Check model numbers listed in the recall notice for affected items.
Probe covers for use during diagnostic ultrasound procedures may have an inadequate barrier at the seams.
Medline is recalling probe cover kits used with ultrasound devices because they may have weak seams that could allow contamination during procedures. This affects specific model numbers sold between December 2017 and May 2023.
The probe covers may have inadequate barriers at the seams, which could allow contaminants to enter the ultrasound gel during procedures. This might lead to potential contamination of the gel and the patient or healthcare worker.
Healthcare professionals and medical facilities that use these probe cover kits for ultrasound procedures. Patients receiving procedures using these kits may be at risk of contamination.
Check the model number on the kit. Affected models include DYNJ64675 through DYNJ907858, sold between December 2017 and May 2023. The product is labeled as a 'Probe Cover Kit' for ultrasound procedures.
Look for the model number on the kit label to determine if it is affected. Affected models are listed in the recall notice.
The recall states that the probe covers may have inadequate barriers at the seams, which could allow contamination during procedures. They are not safe to use as-is.
Check the model number on the kit. Affected models are listed in the recall notice, including DYNJ64675 through DYNJ907858, sold between December 2017 and May 2023.
The recall does not specify a remedy, so you should contact Medline directly for guidance on safe disposal 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-2168-2023 — Medline Medline Hello, I own a Medline that is covered by recall Z-2168-2023 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.
