Medline recalls certain medical procedure convenience kits that may contain non-sterile products if the breather pouch seal is opened. Affected kits include specific models 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 specific medical procedure convenience kits that could allow non-sterile products to be used if the breather pouch seal is opened. This poses a risk of infection or contamination during medical procedures.
The breather pouch seal on certain kits may open or become unsealed, allowing non-sterile products to be used. This could lead to infections or contamination during medical procedures if the seal is compromised.
Healthcare professionals and medical facilities that use these kits are most at risk. Patients undergoing procedures with these kits could be exposed to non-sterile materials.
Check for kits labeled with specific model numbers like CVI4730A, DYNJ20803D, or DYNJ28368. Look for lot numbers such as 24ABK903, 23LBN351, or 24ABE939 on the packaging.
Inspect the breather pouch seal for any signs of being opened or unsealed.
If the seal is open or unsealed, discard the kit immediately to prevent potential contamination.
The recall includes Medline medical procedure convenience kits with model numbers like CVI4730A, DYNJ20803D, and DYNJ28368, and specific lot numbers such as 24ABK903 and 23LBN351.
Check if the breather pouch seal is open or unsealed; if so, the kit may contain non-sterile products and should be discarded immediately.
The recall does not specify a return process, so contact Medline directly for further instructions if the seal is compromised.
We’ve drafted a message you can send Medline to request your refund or repair — edit it as you like.
Subject: Recall Z-0157-2025 — Medline Medline Hello, I own a Medline that is covered by recall Z-0157-2025 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.
