Medline recalls specific medical procedure kits that may contain non-sterile products if the breather pouch seal is opened. Affected kits include lithotomy and gynecological packs with certain 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 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 using the recalled Medline kits are most at risk. Patients receiving procedures with these kits could face infection if non-sterile products are used.
Check for the product labels: Lithotomy Pack (REF DYNJ24362C) or Major Gynecology Laparoscopy (REF DYNJ46774B). Look for lot numbers 24ABG207, 23LBN531, 23LBL712, or 24ABR224 on the packaging.
Inspect the breather pouch seal for any signs of being opened or unsealed.
If the pouch seal is open or unsealed, discard the kit immediately to prevent potential contamination.
Lithotomy Pack (REF DYNJ24362C) and Major Gynecology Laparoscopy (REF DYNJ46774B) kits with lot numbers 24ABG207, 23LBN531, 23LBL712, or 24ABR224.
Check if the breather pouch seal is open or unsealed; if so, the kit may contain non-sterile products.
If the pouch seal is intact, the kit is safe to use as long as it is not opened or unsealed.
We’ve drafted a message you can send Medline to request your refund or repair — edit it as you like.
Subject: Recall Z-0175-2025 — Medline Medline Hello, I own a Medline that is covered by recall Z-0175-2025 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.
