Medline recalls certain Central Catheter Insertion Kits that may contain non-sterile product if the breather pouch seal is opened. Affected kits have lot number 23LBO846.
It has been determined that certain Convenience kits that were packaged in breather pouch lot 323080002 may result in the potential of using non-sterile product if the vendor seal of the pouch is opened/unsealed.
Medline is recalling specific Central Catheter Insertion Kits that could contain non-sterile products if the breather pouch seal is opened. This poses a risk of infection during medical procedures.
The breather pouch seal on these kits may open or become unsealed, allowing non-sterile product to be used. This could lead to infections during medical procedures if the kit is not properly sealed.
Healthcare professionals using the recalled kits are most at risk. Patients undergoing procedures with these kits could face infection risks.
Check for lot number 23LBO84: The kits were sold with this specific lot number. The product is a Central Catheter Insertion Kit with UDI/DI numbers 40653160992944 (each) or 10653160992943 (case).
Ensure the breather pouch seal is intact before use. If opened, do not use the kit.
Lot number 23LBO846.
The kits have UDI/DI numbers 40653160992944 (each) or 10653160992943 (case) and lot number 23LBO846.
Do not use the kit if the breather pouch seal is opened or unsealed.
We’ve drafted a message you can send Medline to request your refund or repair — edit it as you like.
Subject: Recall Z-0162-2025 — Medline Medline Hello, I own a Medline that is covered by recall Z-0162-2025 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.
