Medline recalls specific medical procedure kits that may contain non-sterile products if the breather pouch seal is opened. Affected kits have unique lot numbers and references. Consumers should check their kits for the listed lot numbers and references to determine if they are 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 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 that use these kits are most at risk. Patients undergoing procedures with these kits could face infection if non-sterile products are used.
Check for the product labels: PLASTIC PACK, REF DYNJ42735A; DR SELEM PACK, REF DYNJ43457; or other listed references. Look for lot numbers like 23LBP975, 23LBS052, 24ABF270, etc.
Look for product references and lot numbers listed in the recall notice to determine if your kit is affected.
The breather pouch seal on certain Medline medical procedure kits may open or become unsealed, potentially allowing non-sterile products to be used during medical procedures.
Check the product label for references like DYNJ42735A, DYNJ43457, or other listed references, and look for lot numbers such as 23LBP975, 23LBS052, 24ABF270, etc.
The recall notice does not specify a remedy, so you should check with Medline directly for further instructions.
We’ve drafted a message you can send Medline to request your refund or repair — edit it as you like.
Subject: Recall Z-0165-2025 — Medline Medline Hello, I own a Medline that is covered by recall Z-0165-2025 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.
