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Angiography Procedure Kit Manifolds
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MEDICAL DEVICE RECALLCRITICAL

Angiography Procedure Kit Manifolds

Angiography kit manifolds recalled due to particulate risk in blood circulation.

What to do

Inspect your inventory for kit REF: NCAG62I containing the affected manifolds. Quarantine and return the kits to Medical Action Industries for replacement.

Recalled
Listed
Updated
Recall No.
Z-2792-2026
Agency
FDA
Firm
Medical Action Industries, Inc. 306
Recall ID
99337
Status
ONGOING

Why it was recalled

Medical Action Industries is recalling angiography procedure kits (REF: NCAG62I) containing Medline Namic Angiographic Star Off Handle Manifolds because particulate matter in the fluid path may enter blood circulation and cause vessel blockage.

Is mine affected?

Check the model, lot, or serial number on the device or its packaging. Yours is affected if it matches one below.

Pack Angiography NCMC 3/Cs BANNER, REF: NCAG62I, containing Medline Namic Angiographic Star Off Handle Manifolds

Lot code
342513, 2028, 336758, 2027, 338977
UDI-DI
20809160490416

Where it was sold

Distributed in Arizona and Colorado.

Timeline

  1. Firm initiated recall
  2. Publicly announced
  3. Listed on Recall Canary
  4. Summary updated

Other Foreign Material recalls

Other recent recalls from Medical Action Industries, Inc. 306

All recalls from Medical Action Industries, Inc. 306

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Editorial summary by Recall Canary · summary updated 2026-07-31 · primary source: U.S. Food and Drug Administration · severity reflects the agency's published classification