Medline recalls specific surgical kits with Pure Pouch components that may have weak seals, risking sterility breaches during use. Affected kits include Difficult Airway Tray and Intubation Kits with certain 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 certain surgical convenience kits that contain Pure Pouch components with weak seals. If the seal fails, the sterile contents could become contaminated, which is dangerous during medical procedures.
The Pure Pouch components in these kits have weak seals that may fail during use. If the seal breaks, the sterile contents inside could become contaminated, leading to infections in patients during medical procedures.
Healthcare professionals using the recalled surgical kits are most at risk. Patients undergoing procedures with these kits could face infection if sterility is compromised.
Check for the product names: Medline Difficult Airway Tray W/O Cook (Pack #ACC010578), Medline Adult/Child Intubation Kits (Packs #ACC010616 and #ACC010616H), and others. Look for specific lot numbers and expiration dates listed in the recall notice.
Identify the product name, pack number, and lot number from the recall list to confirm if your kit is affected.
Reach out to Medline directly for guidance on whether your specific kit is recalled and what steps to take next.
The Pure Pouch components in these kits have weak seals that may fail, risking contamination of sterile contents during medical procedures.
Check the product details against the recall list and contact Medline for specific instructions on next steps.
Yes, if the seal fails, the sterile contents could become contaminated, potentially leading to infections in patients during medical procedures.
We’ve drafted a message you can send Medline to request your refund or repair — edit it as you like.
Subject: Recall Z-2230-2024 — Medline Medline Hello, I own a Medline that is covered by recall Z-2230-2024 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.
