Medline recalls Centurion pediatric/adult tracheostomy kits with potential non-sterile product if breather pouch seal is opened. Affected kits have specific lot numbers and model codes.
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 pediatric and adult tracheostomy kits that could contain non-sterile products if the breather pouch seal is broken. This poses a risk of infection during medical procedures.
The breather pouch seal may open during handling, allowing non-sterile product to be used. This could lead to infection if the kit is used without proper sterility.
Patients undergoing tracheostomy procedures and healthcare providers using the kits are most at risk. The recall affects specific lot numbers of the Centurion tracheostomy kits.
Check for lot numbers 23LBM753 or 23KBD877 on the kit packaging. The product code is TC7895 with UDI/DI numbers 40193489435246 (each) or 10193489435245 (case).
Inspect the breather pouch for any signs of opening or damage.
The breather pouch seal may open, allowing non-sterile product to be used during medical procedures.
Lot numbers 23LBM753 and 23KBD877.
Look for lot numbers 23LBM753 or 23KBD877 on the packaging, with product code TC7895.
We’ve drafted a message you can send Medline to request your refund or repair — edit it as you like.
Subject: Recall Z-0148-2025 — Medline Medline Hello, I own a Medline that is covered by recall Z-0148-2025 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.
