Medline recalls probe cover kits containing sterile ultrasound gel that may have inadequate barriers at seams during diagnostic ultrasound procedures. Affected kits include specific models sold between December 2017 and May 2023.
Probe covers for use during diagnostic ultrasound procedures may have an inadequate barrier at the seams.
Medline is recalling probe cover kits that contain sterile ultrasound gel. These kits may have inadequate barriers at the seams, which could lead to contamination during medical procedures. Affected models were sold from December 2017 through May 2023.
The probe covers may have an inadequate barrier at the seams, potentially allowing contaminants to enter the ultrasound gel during procedures. This could lead to infection or other complications for patients.
Healthcare professionals using these kits during diagnostic ultrasound procedures are most at risk. Patients receiving these procedures may also be affected if the kits are used improperly.
Check for the model numbers listed in the recall notice, which include specific identifiers like DYNJ0037936C, DYNJ0037936D, and others. These kits were distributed by Medline between December 2017 and May 2023.
Look for the model numbers listed in the recall notice, such as DYNJ0037936C, DYNJ0037936D, and others.
Reach out to Medline directly for further assistance or to confirm if your kit is affected.
The recall indicates that the probe covers may have inadequate barriers at the seams, which could lead to contamination during procedures. Affected kits should not be used until replaced.
Check the model number on your kit against the list of affected models provided in the recall notice, which includes specific identifiers like DYNJ0037936C, DYNJ0037936D, and others.
These kits were distributed by Medline between December 2017 and 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-2160-2023 — Medline Medline Hello, I own a Medline that is covered by recall Z-2160-2023 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.
