Medline recalls CW PERI GYN convenience kits with model DYNJ80807B due to potential weak seals on breather pouches that could lead to contamination during procedures.
There is a potential for open/weak seals on purchased breather pouches used for packaging of select sterile convenience kits.
Medline is recalling CW PERI GYN convenience kits with model number DYNJ80807B because the breather pouches used for packaging may have weak seals. This could allow contaminants to enter the sterile kits during medical procedures, posing a risk of infection.
The breather pouches that package the sterile kits may have open or weak seals. If these seals fail, contaminants could enter the kits during medical procedures, potentially causing infections.
Healthcare professionals using Medline CW PERI GYN convenience kits with model DYNJ80807B are most at risk. These kits are used for various medical procedures requiring sterile environments.
Check for model number DYNJ80807B on the kit. These kits were sold with lot numbers starting with 24IBH993 and were distributed by Medline Industries, LP in Northfield.
Look for model number DYNJ80807B on the convenience kit packaging.
The breather pouches used for packaging may have open or weak seals, which could allow contaminants to enter the sterile kits during medical procedures.
Check the model number on the kit. If it is DYNJ80807B, contact Medline for instructions on how to handle the kit.
The recall addresses a potential risk of contamination during procedures, not direct injury. The hazard does not involve death or serious injury in normal use.
We’ve drafted a message you can send Medline to request your refund or repair — edit it as you like.
Subject: Recall Z-1612-2025 — Medline Medline Hello, I own a Medline that is covered by recall Z-1612-2025 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.
