Medline recalls specific probe cover kits containing Turkuaz ultrasound gel that may not meet sterility specifications. Affected kits include models DYNJE5900-DYNJEX5900 with listed lot numbers. Consumers should check their kits for these model numbers and lot codes.
Potential for the labeled sterile ultrasound gel component within packs to not meet sterility specifications.
Medline is recalling probe cover kits that contain Turkuaz ultrasound gel which may not meet sterility standards. This could lead to infections if the gel is not sterile during medical procedures.
The ultrasound gel in these kits may not meet sterility specifications, which could lead to infections if used during medical procedures. This is a potential contamination risk rather than an immediate safety hazard.
Healthcare professionals and medical facilities using Medline probe cover kits with Turkuaz ultrasound gel. Those most at risk are users who have the specific model numbers and lot numbers listed in the recall.
Check your Medline probe cover kits for model numbers DYNJE5900 through DYNJEX5900. The lot numbers follow the format 069YYMM0001, where YYMM is the year and month of manufacture.
Identify your kit's model number (DYNJE5900 to DYNJEX5900) and lot number (e.g., 06920030012).
The ultrasound gel in these kits may not meet sterility specifications, which could lead to infections during medical procedures.
Check your kit's model number (DYNJE5900 to DYNJEX5900) and lot number (format 069YYMM0001).
The recall does not specify a remedy, so contact Medline directly for guidance on handling affected kits.
We’ve drafted a message you can send Medline to request your refund or repair — edit it as you like.
Subject: Recall Z-2290-2023 — Medline Medline Hello, I own a Medline that is covered by recall Z-2290-2023 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.
