Medline recalls probe cover kits with potential inadequate seam barriers during ultrasound procedures. Includes specific models and lots from Dec 2017 to May 2023. Contact for return or replacement.
Probe covers for use during diagnostic ultrasound procedures may have an inadequate barrier at the seams.
Medline is recalling specific probe cover kits used with ultrasound devices because they may have weak seams that could allow sterile gel to leak. This could lead to contamination during medical procedures if the covers are not properly sealed.
The probe covers may have inadequate barriers at the seams, which could allow sterile ultrasound gel to leak out during procedures. This leakage might lead to contamination of the patient or equipment if the covers are not properly sealed.
Healthcare providers using these kits for ultrasound procedures are most at risk. Patients receiving ultrasound services may be affected if the covers become contaminated.
Check for model numbers DYNDV2200, DYNDV2397, DYNJ24276C, DYNJ66041, DYNJ66041A, or DYNJ66041B on the kit. These were distributed by Medline between December 2017 and May 2023.
Look for the model numbers listed in the recall notice: DYNDV2200, DYNDV2397, DYNJ24276C, DYNJ66041, DYNJ66041A, or DYNJ66041B.
Reach out to Medline directly for instructions on returning or replacing the affected kits.
The affected models are DYNDV2200, DYNDV2397, DYNJ24276C, DYNJ66041, DYNJ66041A, and DYNJ66041B.
These kits were distributed by Medline between December 2017 and May 2023.
Check the model number on the kit. Affected models include DYNDV2200, DYNDV2397, DYNJ24276C, DYNJ66041, DYNJ66041A, or DYNJ66041B.
We’ve drafted a message you can send Medline to request your refund or repair — edit it as you like.
Subject: Recall Z-2187-2023 — Medline Medline Hello, I own a Medline that is covered by recall Z-2187-2023 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.
