Medline recalls 33 medical procedure kits with potential non-sterile product if breather pouch seal is opened. Check product labels for specific model numbers and lot numbers listed.
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 33 different medical procedure convenience kits that may contain non-sterile products if the breather pouch seal is opened. This could lead to infection or other complications during medical procedures.
The breather pouch in these kits has a seal that may not stay closed properly. If the seal is opened or unsealed, the kit could contain non-sterile products, increasing the risk of infection during medical procedures.
Healthcare professionals and medical facilities that use these kits for procedures. The risk is low for most users since the kits are designed for sterile use and the issue only occurs if the pouch seal is accidentally opened.
Check the product label for model numbers like CYSTO CDS, REF CDS983525D or CYSTO PACK-LF, REF DYNJ25834B. Look for lot numbers such as 24ABW238 or 23KBU714 on the packaging.
Look for model numbers and lot numbers on the product label to confirm if it's part of the recall.
The breather pouch seal may open or unseal, potentially allowing non-sterile products to be used during medical procedures.
Check the product label for model numbers like CYSTO CDS, REF CDS983525D or CYSTO PACK-LF, REF DYNJ25834B and lot numbers such as 24ABW238 or 23KBU714.
The recall does not provide a specific remedy, so contact Medline directly for guidance on handling the 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-0161-2025 — Medline Medline Hello, I own a Medline that is covered by recall Z-0161-2025 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.
