Medline recalls Namic Angiographic Manifolds with particulate in fluid path. Affected units have specific SKUs and lot numbers. Stop using immediately to prevent potential complications.
Medline has identified the presence of particulate within the fluid path of the Manifolds.
Medline is recalling certain Namic Angiographic Manifolds due to particulate matter in the fluid path. This could cause blockages or complications during medical procedures. Affected units have specific SKUs and lot numbers listed in the recall.
Particulate matter in the fluid path may cause blockages or complications during medical procedures. This could lead to issues with blood flow or device function during critical surgeries.
Medical professionals using cardiopulmonary bypass equipment are most at risk. Patients undergoing surgery with these manifolds could face complications.
Check for Medline Product Number/SKU 64038402 or lot numbers 92261, 152082, 163966, 163256. The UDI/DI numbers 10193489059182 and 30193489059186 also identify affected units.
Discard the affected Namic Angiographic Manifold if you have it.
Particulate matter in the fluid path could cause blockages or complications during medical procedures.
Check for Medline Product Number/SKU 64038402 or lot numbers 92261, 152082, 163966, 163256.
Discard the affected Namic Angiographic Manifold immediately.
We’ve drafted a message you can send Medline to request your refund or repair — edit it as you like.
Subject: Recall Z-2140-2026 — Medline Medline Hello, I own a Medline that is covered by recall Z-2140-2026 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.
