Medline recalls Probe Cover Kits with Model DYNJ60126B that may have inadequate seam barriers during ultrasound procedures. Affected kits were sold from Dec 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 with Model DYNJ60126B that may have weak seams, potentially allowing ultrasound gel to leak during procedures. This could lead to contamination or infection risks if the cover isn't properly sealed.
The probe covers may have weak seams that allow ultrasound gel to leak during procedures. This could lead to contamination or infection risks if the cover isn't properly sealed. The risk is low but requires careful handling to prevent potential exposure.
Healthcare professionals using Medline Probe Cover Kits with Model DYNJ60126B for ultrasound procedures are most at risk. Patients receiving these kits during diagnostic ultrasounds may also be affected.
Check for Model Number DYNJ60126B on the kit. These kits were sold by Medline between December 2017 and May 2023. Look for the specific UDI/DI codes listed in the recall notice.
Look for Model Number DYNJ60126B on the probe cover kit.
Reach out to Medline directly for further instructions on the recall.
The model number is DYNJ60126B.
These kits were sold by Medline between December 2017 and May 2023.
Check for Model Number DYNJ60126B and the specific UDI/DI codes listed in the recall notice.
The recall states the covers may have inadequate seam barriers, but no specific injury risks are mentioned.
We’ve drafted a message you can send Medline to request your refund or repair — edit it as you like.
Subject: Recall Z-2174-2023 — Medline Medline Hello, I own a Medline that is covered by recall Z-2174-2023 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.
