Medline recalls 37 convenience kits for cardiac procedures due to potential weak seals on breather pouches that could lead to contamination. Affected kits include specific models and lot numbers.
There is a potential for open/weak seals on purchased breather pouches used for packaging of select sterile convenience kits.
Medline is recalling 37 different convenience kits used in cardiac procedures because some breather pouches might have weak seals. This could lead to contamination of sterile kits during medical procedures.
The breather pouches used to package the kits may have open or weak seals. This could allow contaminants to enter the sterile kit, potentially causing infections or other complications during medical procedures.
Healthcare professionals using these kits for procedures like heart surgery or pacemaker installations are most at risk. Patients receiving these kits during procedures may be affected if contamination occurs.
Check for model numbers listed in the recall: DYNJ59310D, DYNJ32436A, DYNJ35586G, and others. Also look for lot numbers starting with 24IBB643, 24IBG295, and other specific dates.
Identify the model number on the kit packaging to see if it matches the recalled list.
Reach out to Medline customer service for assistance with the recall and to confirm if your kit is affected.
No, only specific kits with model numbers listed in the recall are affected.
The recall states there is a potential for open/weak seals, but no visual inspection method is provided in the record.
Contact Medline directly to confirm if your kit is affected and follow their instructions.
We’ve drafted a message you can send Medline to request your refund or repair — edit it as you like.
Subject: Recall Z-1592-2025 — Medline Medline Hello, I own a Medline that is covered by recall Z-1592-2025 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.
