Medline recalls specific Namic Angiographic Manifolds due to particulate contamination in fluid paths, which could cause blockages during medical procedures.
Medline has identified the presence of particulate within the fluid path of the Manifolds.
Medline is recalling certain Namic Angiographic Manifolds that may contain particulate matter in the fluid path. This could lead to blockages during medical procedures, potentially causing complications for patients.
Particulate matter in the fluid path could block blood flow or cause blockages during critical medical procedures. This risk is specific to the internal fluid pathways of the manifolds used in cardiopulmonary bypass systems.
Healthcare professionals using the recalled manifolds for cardiopulmonary bypass procedures are most at risk. Patients undergoing surgery with these devices may experience complications due to particulate blockages.
Check for the Medline Product Number/SKU 64038200 or Lot Numbers listed: 90184, 94779, 97786, 106351, 108597, 109876, 114056, 114989, 115459, 115931, 116358, 116865, 118245, 122974, 126077, 127795, 129531, 130557, 136114, 150501, 151591, 152772, 154514, 156045, 160318, 163255, 168053.
Verify the Medline Product Number/SKU 64038200 or Lot Numbers listed in the recall notice.
The manifolds may contain particulate matter in the fluid path, which could cause blockages during medical procedures.
Check for the Medline Product Number/SKU 64038200 or Lot Numbers listed: 90184, 94779, 97786, 106351, 108597, 109876, 114056, 114989, 115459, 115931, 116358, 116865, 118245, 122974, 126077, 127795, 129531, 130557, 136114, 150501, 151591, 152772, 154514, 156045, 160318, 163255, 168053.
The recall does not specify an immediate stop-use requirement; however, healthcare professionals should check if they have the recalled items.
We’ve drafted a message you can send Medline to request your refund or repair — edit it as you like.
Subject: Recall Z-2138-2026 — Medline Medline Hello, I own a Medline that is covered by recall Z-2138-2026 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.
