Medline recalls 55 labor and delivery convenience kits with potential weak seals on breather pouches that could lead to contamination. Affected kits include LABOR AND DELIVERY PACK-LF and VAGINAL DELIVERY PACK-LF models. Stop using immediately if you have these kits.
There is a potential for open/weak seals on purchased breather pouches used for packaging of select sterile convenience kits.
Medline is recalling 55 different labor and delivery convenience kits because some breather pouches used to package them may have weak seals. This could allow contamination of sterile kits during use, which is risky for medical procedures.
The breather pouches used to package some sterile convenience kits may have open or weak seals. This could allow contaminants to enter the kit during use, potentially leading to infections or other complications during medical procedures.
Healthcare providers using Medline convenience kits for labor and delivery procedures are most at risk. Patients receiving these kits during childbirth may also be affected if the seals fail.
Check the model numbers listed in the recall: DYNJ26971L, DYNJ0378319P, DYNJ64017B, and others. These kits were sold with specific lot numbers from 2024 (e.g., 24IBD872) through early 2025 (e.g., 25ABA840).
If you have any of the recalled kits, stop using them right away to avoid potential contamination.
No, only specific kits with model numbers listed in the recall (e.g., DYNJ26971L) are affected.
Check the model number on your kit. The affected kits have model numbers like DYNJ26971L, DYNJ0378319P, and others listed in the recall notice.
Stop using the kit immediately and contact Medline for instructions on disposal or replacement.
We’ve drafted a message you can send Medline to request your refund or repair — edit it as you like.
Subject: Recall Z-1611-2025 — Medline Medline Hello, I own a Medline that is covered by recall Z-1611-2025 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.
