Medline recalls medical procedure convenience kits that may allow non-sterile product use if breather pouch vendor seal is opened. Check product labels for specific model numbers and lot numbers to determine if affected.
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 medical procedure convenience kits that could lead to using non-sterile products if the breather pouch's vendor seal is opened. This poses a risk of infection or contamination during medical procedures.
The breather pouches in these kits have a vendor seal that may open or become unsealed, allowing non-sterile products to be used. This could lead to contamination or infection during medical procedures if the seal is compromised.
Healthcare professionals and medical facilities using these kits are most at risk. Patients receiving procedures with these kits could face infection if non-sterile materials are used.
Check the product label for model numbers like CDS982519W, CDS984003A, or DYNJ32639C. Look for lot numbers such as 24BBQ775, 24ABG354, or 23KBE944 on the packaging.
Look for model numbers and lot numbers on the packaging to confirm if the kit is affected.
If the kit has a breather pouch with an unsealed vendor seal, do not use it for medical procedures.
The affected kits include Medline medical procedure convenience kits with model numbers like CDS982519W, CDS984003A, DYNJ32639C, and lot numbers such as 24BBQ775, 24ABG354, or 23KBE944.
The recall states that the breather pouch vendor seal may be opened/unsealed, but the record does not specify how to visually identify this issue.
The recall record does not mention a return or replacement remedy, so no action is required beyond checking the label and not using 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-0179-2025 — Medline Medline Hello, I own a Medline that is covered by recall Z-0179-2025 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.
