Medline recalls three convenience kits with potential weak seals on breather pouches that could lead to contamination during procedures. Affected kits include specific models and lot numbers. Consumers should contact Medline for details.
There is a potential for open/weak seals on purchased breather pouches used for packaging of select sterile convenience kits.
Medline is recalling three specific convenience kits used in medical procedures because the breather pouches might have weak seals. This could lead to contamination during surgeries or other procedures if the pouches fail to seal properly.
The breather pouches used to package the sterile kits may have open or weak seals. If these pouches fail to seal properly, contaminants could enter the sterile field during medical procedures, potentially causing infection or contamination.
Healthcare professionals using the recalled Medline convenience kits for procedures like arthroscopy are most at risk. Patients receiving these kits may also be affected if the seals fail during surgery.
Check for the model numbers DYNJ40229A, OPK382N, or DYNJ46723B on the kit packaging. The lot numbers 24JBM438, 24JBN001, and 24JBQ891 are also associated with these kits.
Reach out to Medline directly for specific instructions on how to handle the recalled kits.
The affected kits include Medline Arthroscopy Du Genou-LF (DYNJ40229A), Arthroscopy Pack-LF (OPK382N), and Arthroscopy New Tegh-LF (DYNJ46723B).
Check for the model numbers DYNJ40229A, OPK382N, or DYNJ46723B and lot numbers 24JBM438, 24JBN001, or 24JBQ891 on the packaging.
Contact Medline directly for specific instructions on handling the recalled kits.
We’ve drafted a message you can send Medline to request your refund or repair — edit it as you like.
Subject: Recall Z-1619-2025 — Medline Medline Hello, I own a Medline that is covered by recall Z-1619-2025 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.
