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 may have particulates in their fluid path that could enter blood circulation and become lodged in blood vessels, posing a risk of blood clots.
The manifolds contain particulates in their fluid path that could enter the bloodstream. If these particles become lodged in blood vessels, they may cause blockages leading to blood clots.
Healthcare professionals using these kits for angiography procedures are most at risk. Patients receiving procedures with the recalled manifolds could potentially be affected.
Check for Halyard convenience kits with Medline Namic Angiographic Star Off Handle Manifolds. The kits have specific serial numbers: SAMM066-15 and UDI-DI 10809160388495.
Look for the serial numbers SAMM066-15 or UDI-DI 10809160388495 on the kit packaging.
The manifolds contain particulates in their fluid path that could enter blood circulation and become lodged in blood vessels.
Check the kit for the serial numbers SAMM066-15 or UDI-DI 10809160388495. If you have these numbers, contact AVID Medical for instructions.
The recall states particulates could enter blood circulation and cause blockages, but the record does not specify if this leads to serious injury in normal use.
We’ve drafted a message you can send AVID Medical to request your refund or repair — edit it as you like.
Subject: Recall Z-2797-2026 — AVID Medical AVID Medical Hello, I own a AVID Medical that is covered by recall Z-2797-2026 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.
