Medline recalls four probe cover kit models with potential inadequate seam barriers during ultrasound procedures. Affected kits include infant insertion packs and maintenance bundles sold from Dec 2017 to May 2023.
Probe covers for use during diagnostic ultrasound procedures may have an inadequate barrier at the seams.
Medline is recalling four types of probe cover kits that may have weak seams where ultrasound gel is applied. This could allow contaminants to enter the body during procedures, posing a risk of infection.
The probe covers may have an inadequate barrier at the seams, which could allow contaminants to enter the body during ultrasound procedures. This poses a risk of infection if the covers are not properly sealed.
Healthcare providers using these kits for infant or adult ultrasound procedures are most at risk. The recall affects kits sold between December 2017 and May 2023.
Check for model numbers: CVI4770A (infant insertion), DT21275 (insertion bundle), EBSI1382 (maintenance), or EBSI1464 (midline dressing). These kits were sold from December 2017 to May 2023.
Look for model numbers CVI4770A, DT21275, EBSI1382, or EBSI1464 on the kit packaging.
Medline will provide replacement kits if you have the affected models.
The recall indicates a potential risk of contamination due to inadequate seam barriers, so they should not be used until replaced.
Check for model numbers CVI4770A, DT21275, EBSI1382, or EBSI1464 on the packaging, which were sold between December 2017 and May 2023.
The recall requires replacement, but you do not need to stop using them immediately—contact Medline for a replacement kit.
We’ve drafted a message you can send Medline to request your refund or repair — edit it as you like.
Subject: Recall Z-2202-2023 — Medline Medline Hello, I own a Medline that is covered by recall Z-2202-2023 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.
