Medline recalls 34 medical procedure convenience kits that may allow non-sterile product use if the breather pouch seal is opened. Affected kits have specific model numbers and lot numbers.
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 34 different medical procedure convenience kits that could allow non-sterile products to be used if the breather pouch seal is opened. This is a risk for medical procedures where sterile products are required.
The breather pouch on these kits has a vendor seal that can be opened or unsealed. If this seal is opened, non-sterile products could be used during medical procedures, which could lead to infections or other complications.
Healthcare professionals and medical facilities that use these kits for procedures like tonsillectomies or other ENT surgeries. The risk is low for most users since the hazard only occurs if the pouch seal is accidentally opened.
Check the product label for model numbers like T&A CDS-LF (REF CDS982091I) or TONSIL CDS (REF CDS984492B). Look for lot numbers such as 24BBA623 or 24ABB114 on the packaging.
Look for model numbers and lot numbers on the kit packaging to confirm if it's affected.
The breather pouch seal on certain kits can be opened or unsealed, potentially allowing non-sterile products to be used during medical procedures.
Check the product label for model numbers like T&A CDS-LF (REF CDS982091I) or TONSIL CDS (REF CDS984492B) and lot numbers such as 24BBA623 or 24ABB114.
The recall does not require immediate action, but you should check the product label to confirm if it's affected. If it is, you may want to contact Medline for further guidance.
We’ve drafted a message you can send Medline to request your refund or repair — edit it as you like.
Subject: Recall Z-0160-2025 — Medline Medline Hello, I own a Medline that is covered by recall Z-0160-2025 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.
