Medline recalls 60+ medical kits with particulate in fluid paths. Affected kits include DBD-MTS, MTS-LEFT HEART, and others. No remedy stated in official notice.
Medline has identified the presence of particulate within the fluid path of the Manifolds.
Medline has recalled 60+ medical kits due to particulate matter in the fluid path of the manifolds. This could cause blockages or complications during medical procedures. The recall is for specific kit models and lot numbers.
The recall states particulate matter is present in the fluid path of the manifolds. This could lead to blockages or complications during medical procedures, such as cardiac catheterizations, where fluid flow is critical.
Healthcare professionals using these kits for procedures like cardiac catheterization are most at risk. Patients using the kits could face complications if particulate matter blocks fluid flow.
Check for Medline kit numbers and SKUs listed in the recall (e.g., 60010195, 60033123). Look for specific lot numbers like 24CBF820, 25BBI613, etc. The kits are used in cardiac procedures.
Identify your Medline kit by SKU (e.g., 60010195) and lot number (e.g., 24CBF820) from the list provided in the recall.
The recall states particulate matter is present in the fluid path of the manifolds, which could cause blockages or complications during medical procedures.
The official notice does not state a remedy, so no action is required beyond checking if your kit is affected.
The affected kits include specific Medline models like DBD-MTS, MTS-LEFT HEART, and others with SKUs listed in the recall (e.g., 60010195, 60033123).
We’ve drafted a message you can send Medline to request your refund or repair — edit it as you like.
Subject: Recall Z-2144-2026 — Medline Medline Hello, I own a Medline that is covered by recall Z-2144-2026 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.
