Medical Action Industries recalls Pack Angiography NCMC 3/Cs BANNER kits with Medline Namic Angiographic Star Off Handle Manifolds due to potential particulate in fluid paths that could enter blood circulation.
Cardiovascular procedure kits contain manifolds, the subject of another recall, that may have particulate within the fluid path, which has the potential to be introduced into blood circulation and become lodged within blood vessels.
Medical Action Industries is recalling certain Pack Angiography kits because their manifolds may contain particles that could enter blood circulation and cause blockages. This is serious for medical procedures involving blood vessels.
The manifolds in these kits may have small particles in the fluid path. If these particles enter the bloodstream during a procedure, they could get stuck in blood vessels, causing blockages or other complications.
Healthcare professionals using these kits for cardiovascular procedures are most at risk. Patients undergoing such procedures with the recalled kits could face complications.
Check for the model 'Pack Angiography NCMC 3/Cs BANNER' with reference number NCAG62I. The lot numbers listed are 342513 (expires 1/16/2028), 336758 (expires 9/20/2027), and 338977 (expires 1/16/2028).
Immediately stop using the recalled Pack Angiography kits if you have them.
The manifolds may contain particles that could enter blood circulation and become lodged in blood vessels during procedures.
Check for the model 'Pack Angiography NCMC 3/Cs BANNER' with reference number NCAG62I and lot numbers 342513, 336758, or 338977.
The recall record does not specify a return process or instructions for disposal.
We’ve drafted a message you can send Medical Action Industries to request your refund or repair — edit it as you like.
Subject: Recall Z-2792-2026 — Medical Action Industries Medical Action Industries Hello, I own a Medical Action Industries that is covered by recall Z-2792-2026 from Medical Action Industries. 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.
