Medline recalls specific medical procedure convenience kits that may contain non-sterile product if the breather pouch seal is opened. Check product labels for 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 certain medical procedure convenience kits that could lead to using non-sterile products if the breather pouch seal is opened. This poses a risk of infection or contamination during medical procedures.
The breather pouch seal on these kits may be opened or unsealed, allowing non-sterile product to be used. This could lead to infections or contamination during medical procedures if the seal is compromised.
Healthcare professionals and medical facilities using the recalled Medline convenience kits. Those handling the kits without checking the seal are at risk of using non-sterile products.
Check product labels for the model codes (e.g., TRAY ADD A CATH FOL UM MF 10ML, REF DYND150200S) and lot numbers (e.g., 23LBK182). The kits were sold with specific breather pouch lot numbers that may have been affected.
Look for model codes and lot numbers on the kit packaging to determine if it is part of the recall.
The breather pouch seal on certain Medline medical procedure kits may be opened or unsealed, potentially allowing non-sterile product to be used.
Check the model codes and lot numbers on the kit packaging. The recalled kits have specific model codes like TRAY ADD A CATH FOL UM MF 10ML, REF DYND150200S and lot numbers such as 23LBK182.
Check the product labels for the model codes and lot numbers to determine if it is part of the recall. If affected, you may need to use alternative kits or follow additional guidance from Medline.
We’ve drafted a message you can send Medline to request your refund or repair — edit it as you like.
Subject: Recall Z-0164-2025 — Medline Medline Hello, I own a Medline that is covered by recall Z-0164-2025 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.
