Medline recalls probe cover kits (models DYNJE5900-5940, DYNJEX5900) for potential inadequate seam barriers during diagnostic ultrasound procedures. All lots within expiry dates 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 probe cover kits for diagnostic ultrasound procedures because the covers may have weak seams that don't protect against fluid exposure. This could lead to contamination or infection risks during medical procedures.
The probe covers may have inadequate barriers at the seams, allowing fluids to leak during ultrasound procedures. This could lead to contamination or infection risks for both medical staff and patients.
Healthcare professionals using these kits during diagnostic ultrasound procedures are most at risk. Patients receiving procedures with these covers could also face infection risks.
Check for model numbers DYNJE5900, DYNJE5910, DYNJE5920, DYNJE5930, DYNJE5940, or DYNJEX5900 on the kit packaging. These kits were sold by Medline between December 2017 and May 2023.
Identify the model number on the kit packaging to confirm if it's one of the recalled models.
Reach out to Medline for guidance on next steps if you have the recalled kit.
The recall states the covers may have inadequate barriers at the seams, so they are not recommended for use until the issue is resolved.
Check for model numbers DYNJE5900, DYNJE5910, DYNJE5920, DYNJE5930, DYNJE5940, or DYNJEX5900 on the packaging. These kits were distributed by Medline between December 2017 and May 2023.
The recall does not specify a remedy, so contact Medline directly for guidance on next steps.
We’ve drafted a message you can send Medline to request your refund or repair — edit it as you like.
Subject: Recall Z-2154-2023 — Medline Medline Hello, I own a Medline that is covered by recall Z-2154-2023 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.
