Medline recalls probe cover kits with potential inadequate seam barriers during ultrasound procedures. Affected kits include specific models from December 2017 to May 2023. Consumers should check model numbers and 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 that may have weak seams, risking contamination during ultrasound procedures. This could lead to infections or other complications if the barrier fails. Affected kits were sold between December 2017 and May 2023.
The probe covers may have an inadequate barrier at the seams, which could allow contaminants to enter the ultrasound gel during procedures. This increases the risk of infection or other complications for patients and healthcare workers.
Healthcare professionals using these kits for ultrasound procedures are most at risk. Patients receiving procedures with these kits could also be affected if the barrier fails.
Check the model number on the kit: CDS983069I, DYNJ30245, DYNJ47716B, DYNJ63347A, DYNJ63634A, DYNJ81389A, DYNJ83960, or DYNJ907206D. Kits were sold by Medline between December 2017 and May 2023.
Look for the model number on the kit: CDS983069I, DYNJ30245, DYNJ47716B, DYNJ63347A, DYNJ63634A, DYNJ81389A, DYNJ83960, or DYNJ907206D.
Reach out to Medline for further instructions on how to return or replace the kit.
Affected model numbers include CDS983069I, DYNJ30245, DYNJ47716B, DYNJ63347A, DYNJ63634A, DYNJ81389A, DYNJ83960, and DYNJ907206D.
These kits were distributed by Medline between December 2017 and May 2023.
Check the model number on the kit. Affected kits have specific model numbers listed in the recall notice.
We’ve drafted a message you can send Medline to request your refund or repair — edit it as you like.
Subject: Recall Z-2172-2023 — Medline Medline Hello, I own a Medline that is covered by recall Z-2172-2023 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.
