Medline brand medical procedure convenience kits with specific model numbers and lot numbers may have non-sterile product if the vendor seal is opened. Affected kits include L&D/OB PACK-LF and VAG DELIVERY HLTH models.
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 medical procedure convenience kits labeled as L&D/OB PACK-LF or VAG DELIVERY HLTH may have non-sterile products if the vendor seal of the breather pouch is opened. This could lead to infection or contamination during medical procedures.
The breather pouches in these kits were packaged with a vendor seal that may not stay sealed properly. If the seal is opened or unsealed, non-sterile product could be used during medical procedures, potentially causing infection or contamination.
Healthcare providers and medical facilities that use these kits for labor and delivery procedures are most at risk. The specific kits listed in the recall are used in obstetrics and gynecology settings.
Check for kits labeled as L&D/OB PACK-LF or VAG DELIVERY HLTH with specific model numbers and lot numbers listed in the recall. The kits include model references like DYNJ0213264O and DYNJ0375486K.
Inspect the vendor seal on the breather pouch for any signs of being opened or unsealed.
No, but you should check the vendor seal on the breather pouch to ensure it hasn't been opened or unsealed.
If the seal is opened or unsealed, non-sterile product may be used, which could lead to infection or contamination during medical procedures.
Check the product label for specific model numbers and lot numbers listed in the recall, such as DYNJ0213264O or DYNJ0375486K.
We’ve drafted a message you can send Medline to request your refund or repair — edit it as you like.
Subject: Recall Z-0174-2025 — Medline Medline Hello, I own a Medline that is covered by recall Z-0174-2025 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.
Experiences, tips, and questions from readers. Every comment is reviewed before it appears.
No comments yet — be the first to share your experience.
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.
