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Stop using now Medical device recall · FDA · Published May 13, 2026

Medical Action Industries Pack Angiography Kits Risk Blood Clots from Particulate

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.

Plain-English summary generated from official FDA data by GovInfoNow · Published by Carlos Caban · How we make summaries

🇺🇸 FDA recall #Z-2792-2026Medical deviceMedical Action Industries ›
✎ GovInfoNow plain-language explainer

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. Read more at govinfonow.com/recall/169448-medical-action-industries-pack-angiography-kits-risk-blood-clots-from.

Source Summary by GovInfoNow · govinfonow.com/recall/169448-medical-action-industries-pack-angiography-kits-risk-blood-clots-from · Updated August 17, 2026 · FDA enforcement record: FDA #Z-2792-2026

Cite this page

“Medical Action Industries Pack Angiography Kits Risk Blood Clots from Particulate.” GovInfoNow, updated August 17, 2026. https://govinfonow.com/recall/169448-medical-action-industries-pack-angiography-kits-risk-blood-clots-from. Based on FDA recall #Z-2792-2026 (https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2792-2026%22&limit=1).

The FDA announced on May 13, 2026, that Medical Action Industries is recalling Pack Angiography NCMC 3/Cs BANNER kits containing manifolds that may have particulates. The hazard involves potential introduction of these particles into blood circulation. This Class I recall affects 657 units distributed in Arizona and Colorado.

How to tell if you have it

  • Brand: Medical Action Industries
  • Product: Pack Angiography NCMC 3/Cs BANNER, REF: NCAG62I
  • UDI-DI: 20809160490416
  • Lot/Expiration: 342513(1/16/2028), 336758(9/20/2027), 338977(1/16/2028)

The hazard

According to the FDA, the cardiovascular procedure kits contain manifolds that may have particulate within the fluid path. This particulate has the potential to be introduced into blood circulation and become lodged within blood vessels.

Context

GovInfoNow's records show Medical Action Industries, Inc. 306 has 14 other recalls on record since 2019-12-02. Other recent recalls of similar products include AVID Medical Halyard Kits Recall: Particulates Risk Blood Clots (2026-04-30) and Medline Medical Kits Recall: Particulate in Fluid Path Risk (2026-03-24).

How to tell if you have this one

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).

  • Brand
    Medical Action Industries
  • Category
    Medical device
Based on the official FDA remedy

What to do — step by step

  1. Stop Using Now

    Immediately stop using the recalled Pack Angiography kits if you have them.

Where it went and when

Where it was distributed

Distributed in Arizona and Colorado.

Alaska: not listedAKMaine: not listedMEVermont: not listedVTNew Hampshire: not listedNHWashington: not listedWAIdaho: not listedIDMontana: not listedMTNorth Dakota: not listedNDMinnesota: not listedMNIllinois: not listedILWisconsin: not listedWIMichigan: not listedMINew York: not listedNYRhode Island: not listedRIMassachusetts: not listedMAOregon: not listedORNevada: not listedNVWyoming: not listedWYSouth Dakota: not listedSDIowa: not listedIAIndiana: not listedINOhio: not listedOHPennsylvania: not listedPANew Jersey: not listedNJConnecticut: not listedCTCalifornia: not listedCAUtah: not listedUTColorado: yesCONebraska: not listedNEMissouri: not listedMOKentucky: not listedKYWest Virginia: not listedWVVirginia: not listedVAMaryland: not listedMDDelaware: not listedDEArizona: yesAZNew Mexico: not listedNMKansas: not listedKSArkansas: not listedARTennessee: not listedTNNorth Carolina: not listedNCSouth Carolina: not listedSCDistrict of Columbia: not listedDCOklahoma: not listedOKLouisiana: not listedLAMississippi: not listedMSAlabama: not listedALGeorgia: not listedGAHawaii: not listedHITexas: not listedTXFlorida: not listedFL

FDA distribution: “US: AZ, CO” States read from FDA’s own wording; “not listed” means the notice does not name it.

States: Arizona, Colorado.

Recall timeline

FDA published this recall 3 months after the firm started it.

1. Firm started the recall: May 13, 202612. FDA classified it Class I: Jul 30, 202623. Published in FDA’s Enforcement Report: Aug 5, 202634. Added to GovInfoNow: Aug 11, 202642026
  1. Firm started the recall
  2. FDA classified it Class I
  3. Published in FDA’s Enforcement Report
  4. Added to GovInfoNow

Dates from the agency record only; steps without a date are left out.

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Where this comes from

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.

  • Official source: FDA Recall #Z-2792-2026 (May 13, 2026) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-2792-2026 to see it in context.
  • Plain-language summary written by qwen3:4b on August 17, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
  • GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.
GovInfoNow is an independent guide. We are not FDA or any government agency. Always confirm details with the official recall.Data: CPSC · FDA · NHTSA · USDA