Medline recalls ambulatory mini packs with lot 23LBO804 due to potential non-sterile product if pouch seal is opened. Affected kits may be used in medical procedures without sterile conditions.
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 ambulatory mini packs with lot number 23LBO804 because the breather pouch seal could be opened, risking non-sterile product use during medical procedures. This affects healthcare workers using the kits for procedures requiring sterile conditions.
The breather pouch seal on these kits may open unintentionally, allowing non-sterile product to be used in medical procedures. This could lead to infections or complications if the kit is used without proper sterility.
Healthcare workers using Medline ambulatory mini packs for medical procedures are most at risk. The recall applies to kits with lot number 23LBO804 sold in the U.S.
Check the lot number on the product label; affected kits have lot number 23LBO804. The product is a Medline Ambulatory Mini Pack with reference number DYNJ82579.
Inspect the breather pouch seal for any signs of being opened or unsealed.
Reach out to Medline for guidance on whether the kit needs to be discarded or replaced.
The breather pouch seal may open, risking non-sterile product use during medical procedures.
Lot number 23LBO804.
No, but you should check the pouch seal and contact Medline for specific guidance.
We’ve drafted a message you can send Medline to request your refund or repair — edit it as you like.
Subject: Recall Z-0172-2025 — Medline Medline Hello, I own a Medline that is covered by recall Z-0172-2025 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.
