Medline recalls convenience kits with weak breather pouch seals that may allow contamination. Affected kits include CSTM PACEMAKER DRA: DYNJCD0339 model. Stop using immediately to prevent infection risks.
There is a potential for open/weak seals on purchased breather pouches used for packaging of select sterile convenience kits.
Medline is recalling convenience kits used for medical procedures because the breather pouches might have weak seals that could let contaminants enter. This could lead to infections if the kits are used improperly.
The breather pouches in the kits may have open or weak seals that allow contaminants to enter the sterile packaging. This could lead to infections if the kits are used without proper sterility.
Healthcare professionals using Medline convenience kits for procedures like pacemaker drapes are most at risk. Patients receiving these kits could also be affected if the seals fail during use.
Check for the model number DYNJCD0339 on the kit. The lot number 24KBK055 and UDI-DI numbers 10195327483753 and 40195327483754 are also associated with this recall.
Look for the model number DYNJCD0339 on the convenience kit.
If you have the recalled model, stop using the kit to prevent contamination risks.
The model number is DYNJCD0339.
The lot number is 24KBK055.
Check for the model number DYNJCD0339 and lot number 24KBK055 on the kit.
We’ve drafted a message you can send Medline to request your refund or repair — edit it as you like.
Subject: Recall Z-1607-2025 — Medline Medline Hello, I own a Medline that is covered by recall Z-1607-2025 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.