Medline recalls non-sterile convenience kits with weak seals that could breach sterility. Affected kits have specific pack numbers and expiration dates. Consumers should contact Medline for details.
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 convenience kits that contain a Pure Pouch with weak seals. If the seal fails, the sterility of the contents could be compromised, which is dangerous for medical procedures.
The Pure Pouch component in these kits has weak seals that may fail, leading to a breach in sterility. This could result in infections or complications during medical procedures if the kit is used without proper sterility.
Healthcare professionals using Medline Open Heart CDS kits with the specified pack numbers and expiration dates are most at risk. Patients undergoing surgery could be affected if the kits are used without sterility.
Check for pack numbers CDS981759C with expiration dates listed in the description. The kits contain specific lot numbers and expiration dates, such as 7/31/2025 or 10/31/2025.
Identify the pack number and expiration date on the kit to confirm if it matches the recalled items.
Reach out to Medline for further instructions on how to handle the recalled kits.
The Pure Pouch component has weak seals that may fail, risking a breach in sterility during medical procedures.
Check the pack number and expiration date. Contact Medline for specific instructions on handling the recalled kits.
Yes, a seal failure could compromise sterility, leading to infections or complications during surgery.
We’ve drafted a message you can send Medline to request your refund or repair — edit it as you like.
Subject: Recall Z-2231-2024 — Medline Medline Hello, I own a Medline that is covered by recall Z-2231-2024 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.
