Medline recalls IV Pack South convenience kits with potential weak seals on breather pouches that could lead to contamination during medical procedures.
There is a potential for open/weak seals on purchased breather pouches used for packaging of select sterile convenience kits.
Medline is recalling IV Pack South convenience kits (model DYNJ88422) because their breather pouches might have weak seals. This could allow contaminants to enter the sterile kits during medical procedures, posing a risk to patient safety.
The breather pouches used to package these sterile kits may have open or weak seals. If the seal fails during use, contaminants could enter the kit, potentially causing infections or other complications in medical procedures.
Healthcare professionals using Medline IV Pack South convenience kits (model DYNJ88422) are most at risk. Patients receiving procedures using these kits could be exposed to contamination.
Check for the model number DYNJ88422 on the kit. These kits were sold with lot numbers starting with 24KBD426. They were distributed as IV Pack South convenience kits for medical procedures.
Inspect the breather pouches for any signs of open or weak seals before use.
The recall is due to a potential for open or weak seals on breather pouches used for packaging sterile convenience kits, which could lead to contamination during medical procedures.
The affected model is DYNJ88422 for IV Pack South convenience kits.
Look for the model number DYNJ88422 on the kit and lot numbers starting with 24KBD426.
We’ve drafted a message you can send Medline to request your refund or repair — edit it as you like.
Subject: Recall Z-1604-2025 — Medline Medline Hello, I own a Medline that is covered by recall Z-1604-2025 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.