Medline recalls convenience kits with potential leaks and breakage that could harm patients. Affected kits include specific filter and anesthetic circuit models from 2008. Stop using immediately to prevent health risks.
Medical convenience kits contain plastic syringes affected by the FDA Safety Alert issued on March 19, 2024. Leaks, breakage, and/ other quality issues have been identified that may pose a risk to patient health.
Medline is recalling convenience kits that may leak or break, posing a risk to patient health. These kits have been identified as unsafe due to quality issues and are being taken off the market to protect users.
The kits contain plastic syringes that can leak or break, potentially causing harm to patients. This issue was identified through an FDA safety alert from March 2024.
Healthcare workers and patients using the recalled Medline convenience kits are at risk. Those with the specific filter or anesthetic circuit models from 2008 are most affected.
Check for kits labeled 'FILTER-.8 MICRON' with Pack Number 2008 or 'ANES CIRCUIT 90IN EXP-LF' with specific pack numbers and lot numbers listed in the recall notice.
Discontinue use of the recalled Medline convenience kits to prevent potential leaks or breakage that could harm patients.
The affected models are Medline Convenience kits labeled 'FILTER-.8 MICRON' with Pack Number 2008 and 'ANES CIRCUIT 90IN EXP-LF' with specific pack numbers and lot numbers.
The recall is due to leaks and breakage in the plastic syringes, which could pose a risk to patient health as identified by an FDA safety alert from March 2024.
The recall notice does not specify a return process, but you should stop using them immediately to prevent potential harm.
We’ve drafted a message you can send Medline to request your refund or repair — edit it as you like.
Subject: Recall Z-3031-2024 — Medline Medline Hello, I own a Medline that is covered by recall Z-3031-2024 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.
