Medline recalls probe cover kits with sterile ultrasound gel that may have inadequate seam barriers, risking contamination during diagnostic procedures. Affected kits include specific models 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 probe cover kits that contain sterile ultrasound gel. These kits may have an inadequate barrier at the seams, potentially allowing contamination during diagnostic procedures. Affected models were sold from December 2017 through May 2023.
The probe covers may have an inadequate barrier at the seams during use, which could allow contamination of the sterile ultrasound gel. This poses a risk of infection or cross-contamination during diagnostic procedures if the covers are not properly sealed.
Healthcare professionals using ultrasound equipment are most at risk. Patients undergoing diagnostic ultrasound procedures could be exposed to contamination if the probe covers are used without proper barrier protection.
Check for model numbers: DYNJ44410G, DYNJ9048708I, PHS762887001B, or TVS4700. These kits were sold by Medline between December 2017 and May 2023.
Look for model numbers on the kit: DYNJ44410G, DYNJ9048708I, PHS762887001B, or TVS4700.
If you have an affected model, contact Medline directly for a replacement kit.
Affected models include VNUS TRAY (DYNJ44410G), INTRAUTERINE TRNSFUSION -LF (DYNJ9048708I), PERI NEURO BLOCK PACK-LF (PHS762887001B), and TVS4700 (TVS4700).
These kits were sold by Medline between December 2017 and May 2023.
Check the model number on the kit. Affected models are DYNJ44410G, DYNJ9048708I, PHS762887001B, or TVS4700.
We’ve drafted a message you can send Medline to request your refund or repair — edit it as you like.
Subject: Recall Z-2196-2023 — Medline Medline Hello, I own a Medline that is covered by recall Z-2196-2023 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.
