Medline recalls probe cover kits with potential inadequate seam barriers during ultrasound procedures. Affected kits include specific models from December 2017 to May 2023. Contact Medline for details.
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 weak seams, risking contamination during ultrasound procedures. This could lead to infections or other complications if the covers fail to protect the skin properly.
The probe covers may have an inadequate barrier at the seams, which could allow contaminants to enter the skin during ultrasound procedures. This poses a risk of infection or other complications if the covers fail to protect the skin properly.
Healthcare professionals using these kits for ultrasound procedures are most at risk. Patients receiving procedures with these kits could be exposed to potential contamination.
Check for model numbers listed in the recall: DYNJRA1755, DYNJTESTCFP4, IV8635D, IVS3300, IVS3485A, IVS3825, IVS3840A, MNS11625, MNS7695A, NG410A, PHS41739A, PHS479840M, SYNJ10303B, TVS4500A, TVS4500B, or VC-PK. These kits were distributed between December 2017 and May 2023.
Look for the specific model numbers listed in the recall to determine if your kit is affected.
Reach out to Medline directly for further instructions on how to return or replace the affected kits.
The affected models include DYNJRA1755, DYNJTESTCFP4, IV8635D, IVS3300, IVS3485A, IVS3825, IVS3840A, MNS11625, MNS7695A, NG410A, PHS41739A, PHS479840M, SYNJ10303B, TVS4500A, TVS4500B, and VC-PK.
These kits were distributed by Medline between December 2017 and May 2023.
Check the model number on your kit against the list provided in the recall. Affected kits were distributed between December 2017 and May 2023.
We’ve drafted a message you can send Medline to request your refund or repair — edit it as you like.
Subject: Recall Z-2181-2023 — Medline Medline Hello, I own a Medline that is covered by recall Z-2181-2023 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.
Experiences, tips, and questions from readers. Every comment is reviewed before it appears.
No comments yet — be the first to share your experience.
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.
