Medline recalls non-sterile convenience kits with Pure Pouch components that have weak seals, risking sterility breaches. Affected kits include specific models and lot numbers.
Surgical convenience kits containing Pure Pouch component that has weak seals which may result in a breach in sterility of the contents if the seal fails.
Medline is recalling non-sterile surgical convenience kits that contain Pure Pouch components with weak seals. If the seal fails, the contents could become contaminated, posing a risk of infection during medical procedures.
The Pure Pouch components in these kits have weak seals that may fail, leading to breaches in sterility. If the seal breaks, the contents could become contaminated, increasing infection risk during medical procedures.
Healthcare professionals using these kits in surgical settings are most at risk. Patients undergoing procedures with contaminated kits could face infection.
Check for Medline kits with specific model numbers and lot numbers listed in the recall notice. The kits include items like CC Drawer 4 IV Circulation, Code Cart Drawer 2 Adult Kit, and others with Pure Pouch components.
Identify the product model and lot numbers from the recall list to confirm if your kit is affected.
Reach out to Medline directly for assistance with the recall process or to confirm if your kit is affected.
The Pure Pouch components in these kits have weak seals that may fail, leading to sterility breaches and potential infection risks during medical procedures.
Check for specific model numbers and lot numbers listed in the recall notice, such as Medline CC Drawer 4 IV Circulation (Pack #ACC010254B) or Code Cart Drawer 2 Adult Kit (Pack ACC010365A).
Contact Medline directly to confirm if your kit is affected and follow their instructions for the recall process.
We’ve drafted a message you can send Medline to request your refund or repair — edit it as you like.
Subject: Recall Z-2232-2024 — Medline Medline Hello, I own a Medline that is covered by recall Z-2232-2024 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.
