Medline recalls certain probe cover kits for ultrasound procedures due to potential inadequate barrier at seams. These kits may allow contaminants to enter during use, posing a risk of infection. Affected kits were distributed from December 2017 to May 2023.
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 the covers might have weak seams that could let contaminants get through. This could lead to infections during medical procedures if the covers are not properly sealed.
The probe covers may have seams that are not sealed properly, allowing contaminants to enter during ultrasound procedures. This could increase the risk of infection for patients and healthcare workers if the covers are not used correctly.
Healthcare professionals using Medline's probe cover kits for ultrasound procedures are most at risk. Patients undergoing these procedures could be affected if the covers are used on contaminated surfaces.
Check for model numbers CVI4510, STCVC01145B, or STCVC2000 on the kit. These kits were distributed between December 2017 and May 2023 by Medline.
Look for model numbers CVI4510, STCVC01145B, or STCVC2000 on the probe cover kit.
The recall indicates a potential risk of inadequate barrier at seams, so these kits should not be used until the remedy is applied.
Check the model number on the kit. If it matches CVI4510, STCVC01145B, or STCVC2000, contact Medline for instructions.
These kits were distributed by Medline 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-2195-2023 — Medline Medline Hello, I own a Medline that is covered by recall Z-2195-2023 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.
