Medline recalls probe cover kits with sterile ultrasound gel that may have weak seams, risking contamination during medical procedures. All models from Dec 2017 to May 2023 are affected.
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 weak seams that could allow contamination during medical procedures if used improperly.
The probe covers may have inadequate barriers at the seams, which could allow contaminants to enter the ultrasound gel. This might lead to infection or cross-contamination during medical procedures if the covers are not properly sealed.
Healthcare professionals using these kits for diagnostic ultrasound procedures are most at risk. Patients receiving these procedures may also be affected if the kits are used without proper care.
Check for model numbers listed in the recall: DYNJ83105 through SYNJ10303C. These kits were sold by Medline between December 2017 and May 2023.
Look for model numbers on the kit packaging: DYNJ83105, DYNJ83251, DYNJ83508, DYNJ83656, DYNJ83696, DYNJ83746, DYNJ83815, DYNJ83918, DYNJ83936, DYNJ84040, DYNJ84190, DYNJ902507C, DYNJ902507D, DYNJ905151B, DYNJ906766B, DYNJ908249A, DYNJ909267, DYNJVB1000, or SYNJ10303C.
The probe covers may have inadequate barriers at the seams, which could allow contaminants to enter the ultrasound gel during medical procedures.
Check the model number on the packaging. If it matches the listed models, stop using it and contact Medline for instructions.
Yes, the weak seams could lead to contamination during medical procedures, which might cause infection or cross-contamination.
We’ve drafted a message you can send Medline to request your refund or repair — edit it as you like.
Subject: Recall Z-2162-2023 — Medline Medline Hello, I own a Medline that is covered by recall Z-2162-2023 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.
