Medline recalls probe cover kits with sterile ultrasound gel that may have inadequate seams, risking contamination during 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 containing sterile ultrasound gel because the covers may have weak seams that could allow contamination during medical procedures. This poses a risk of infection or improper treatment if the gel is exposed to contaminants.
The probe covers may have inadequate barriers at the seams, allowing contaminants to enter the sterile ultrasound gel. This could lead to infections or improper treatment during medical procedures if the gel is exposed to unsterile environments.
Healthcare providers using these kits for diagnostic ultrasound procedures are most at risk. Patients receiving treatments with these kits could be exposed to contamination if the covers fail.
Check for model numbers listed in the recall: DYNJ81722, DYNJRA0827A, DYNJRA0881, DYNJRA0881A, DYNJRA1603, DYNJRA1739A, DYNJRA1823, DYNJRA1837, DYNJRA1847, DYNJRA1864, DYNJRA1869, DYNJRA1878, DYNJRA1893, DYNJRA1900, DYNJRA1945, DYNJRA1975, DYNJRA1998, DYNJRA2013, DYNJRA2022, DYNJRA2027, DYNJRA2028, DYNJRA2028A, DYNJRA2041, DYNJRA2044, DYNJRA2086, DYNJRA2148, DYNJRA9040, DYNJRA9044, PAIN1560, PAIN1762. All kits distributed between December 2017 and May 2023 are affected.
Look for model numbers listed in the recall: DYNJ81722, DYNJRA0827A, DYNJRA0881, DYNJRA0881A, DYNJRA1603, DYNJRA1739A, DYNJRA1823, DYNJRA1837, DYNJRA1847, DYNJRA1864, DYNJRA1869, DYNJRA1878, DYNJRA1893, DYNJRA1900, DYNJRA1945, DYNJRA1975, DYNJRA1998, DYNJRA2013, DYNJRA2022, DYNJRA2027, DYNJRA2028, DYNJRA2028A, DYNJRA2041, DYNJRA2044, DYNJRA2086, DYNJRA2148, DYNJRA9040, DYNJRA9044, PAIN1560, PAIN1762.
If you have any of the recalled model numbers, stop using the kits immediately to avoid potential contamination during procedures.
The recall includes model numbers DYNJ81722, DYNJRA0827A, DYNJRA0881, DYNJRA0881A, DYNJRA1603, DYNJRA1739A, DYNJRA1823, DYNJRA1837, DYNJRA1847, DYNJRA1864, DYNJRA1869, DYNJRA1878, DYNJRA1893, DYNJRA1900, DYNJRA1945, DYNJRA1975, DYNJRA1998, DYNJRA2013, DYNJRA2022, DYNJRA2027, DYNJRA2028, DYNJRA2028A, DYNJRA2041, DYNJRA2044, DYNJRA2086, DYNJRA2148, DYNJRA9040, DYNJRA9044, PAIN1560, and PAIN1762.
All affected kits were distributed between December 2017 and May 2023.
Check the model number on the kit. If it matches any of the listed model numbers (DYNJ81722, DYNJRA0827A, etc.), it is affected.
We’ve drafted a message you can send Medline to request your refund or repair — edit it as you like.
Subject: Recall Z-2156-2023 — Medline Medline Hello, I own a Medline that is covered by recall Z-2156-2023 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.
