Medline recalls probe cover kits containing sterile ultrasound gel with potential seam barrier issues that could lead to contamination during diagnostic procedures. Affected models sold from Dec 2017-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 may have inadequate barriers at seams during ultrasound procedures. This could allow contaminants to enter the patient's body during diagnostic procedures, posing a risk of infection.
The probe covers may have an inadequate barrier at the seams, potentially allowing contaminants to enter the patient's body during diagnostic ultrasound procedures. This could lead to infection or other complications.
Healthcare professionals using these probe covers during diagnostic ultrasound procedures. Patients undergoing such procedures with the recalled kits are at risk of contamination.
Check for model numbers listed in the recall: DYNJ906102G, DYNJ906102I, DYNJ906108C, and other specific models sold between December 2017 and May 2023.
Look for model numbers on the product label: DYNJ906102G, DYNJ906102I, DYNJ906108C, and other specific models listed in the recall.
The probe covers may have an inadequate barrier at the seams, potentially allowing contaminants to enter the patient's body during diagnostic ultrasound procedures.
Check the model number on the product label: DYNJ906102G, DYNJ906102I, DYNJ906108C, and other specific models sold between December 2017 and May 2023.
The recall does not specify a remedy, so contact Medline directly for guidance on safe handling or disposal.
We’ve drafted a message you can send Medline to request your refund or repair — edit it as you like.
Subject: Recall Z-2166-2023 — Medline Medline Hello, I own a Medline that is covered by recall Z-2166-2023 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.
