AVID Medical recalls Halyard convenience kits with Medline Namic Angiographic Star Off Handle Manifolds due to particulates that could enter blood circulation and cause blockages.
Affected kits contain Medline Namic Angiographic Star Off Handle Manifolds, which were recalled by the manufacturer due to presence of particulates within fluid path of the Manifolds. Particulate within the fluid path has the potential to be introduced into blood circulation and become lodged within blood vessels.
AVID Medical is recalling Halyard convenience kits that contain Medline Namic Angiographic Star Off Handle Manifolds. These parts have particulates in their fluid path that could enter blood circulation and become lodged in blood vessels, posing a risk of blockages.
Particulates in the fluid path of the manifolds can enter the bloodstream during procedures. If lodged in blood vessels, these particles could cause blockages that might lead to serious complications.
Healthcare professionals using these kits for cardiac catheterization procedures are most at risk. Patients receiving procedures with these kits could also be affected.
Check for Halyard convenience kits labeled 'CARDIAC CATH PACK EAMC1000-05' with specific lot numbers listed in the recall notice.
Identify the lot numbers on your kit: 1573593, 1583827, 1609541, 1612134, 1612516, 1619132, 1623384, 1627013, 1635459, 1672306, 1675159.
Particulates in the fluid path can enter blood circulation and become lodged in blood vessels, potentially causing blockages.
Check for Halyard convenience kits labeled 'CARDIAC CATH PACK EAMC1000-05' with lot numbers from the list: 1573593, 1583827, 1609541, 1612134, 1612516, 1619132, 1623384, 1627013, 1635459, 1672306, 1675159.
The recall does not require immediate stop use; check lot numbers to determine if your kit is affected.
We’ve drafted a message you can send AVID Medical to request your refund or repair — edit it as you like.
Subject: Recall Z-2796-2026 — AVID Medical AVID Medical Hello, I own a AVID Medical that is covered by recall Z-2796-2026 from AVID Medical. 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.
