Medline recalls specific ultrasound probe cover kits with potential inadequate seam barriers. These kits may pose a risk during diagnostic procedures. Affected models were distributed from December 2017 to May 2023.
Probe covers for use during diagnostic ultrasound procedures may have an inadequate barrier at the seams.
Medline is recalling ultrasound probe cover kits that may have weak seams, potentially allowing fluid to leak during procedures. This could lead to contamination or infection risks for patients and healthcare workers.
The probe covers may have an inadequate barrier at the seams, which could allow bodily fluids to leak during ultrasound procedures. This might lead to contamination or infection risks for patients and healthcare workers.
Healthcare providers using these kits for diagnostic ultrasound procedures are most at risk. Patients undergoing procedures with these kits may face contamination or infection.
Check for model numbers listed in the recall: CDS840214Q, DYNDA2418, DYNJ0365463J, and others. These kits were distributed between December 2017 and May 2023.
Identify the model number on the kit to see if it matches the recalled list: CDS840214Q, DYNDA2418, DYNJ0365463J, etc.
Reach out to Medline directly for assistance with replacement or return options.
The recall states the probe covers may have an inadequate barrier at the seams, which could lead to contamination or infection risks. Use with caution.
Check the model number on the kit. Recalled models include CDS840214Q, DYNDA2418, DYNJ0365463J, and others. These kits were distributed between December 2017 and May 2023.
Contact Medline directly for assistance with replacement or return options. The recall does not specify a deadline for action.
We’ve drafted a message you can send Medline to request your refund or repair — edit it as you like.
Subject: Recall Z-2169-2023 — Medline Medline Hello, I own a Medline that is covered by recall Z-2169-2023 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.
