Medline recalls pediatric ultrasound probe cover kits with potential inadequate seam barriers. These kits may pose a risk during diagnostic procedures. Affected kits include model DYNJ45158A distributed 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 pediatric ultrasound probe cover kits that may have an inadequate barrier at the seams. This could allow ultrasound gel to leak during procedures, potentially causing contamination or injury. Affected kits include model DYNJ45158A sold between December 2017 and May 2023.
The probe covers may have an inadequate barrier at the seams, allowing ultrasound gel to leak during procedures. This could lead to contamination or injury if the gel comes into contact with sensitive areas. The risk is specific to pediatric use cases where the gel might leak into the patient's skin.
Healthcare professionals using pediatric ultrasound equipment and patients undergoing diagnostic procedures are most at risk. The recall applies to Medline's pediatric probe cover kits with specific model and distribution dates.
Check for the model number DYNJ45158A on the probe cover kit. The kits were distributed by Medline from December 2017 through May 2023. All lots within the expiry date are affected.
Verify the model number on the probe cover kit to ensure it matches DYNJ45158A.
Reach out to Medline directly for guidance on replacement or alternative solutions.
The affected model number is DYNJ45158A.
The kits were distributed by Medline between December 2017 and May 2023.
Check for the model number DYNJ45158A on the probe cover kit. The kits were distributed from December 2017 through May 2023.
We’ve drafted a message you can send Medline to request your refund or repair — edit it as you like.
Subject: Recall Z-2157-2023 — Medline Medline Hello, I own a Medline that is covered by recall Z-2157-2023 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.
