FDAClass I · Medical device · Recall Z-2792-2026 · Recalled August 5, 2026

Pack Angiography NCMC 3/Cs BANNER recall — Medical Action Industries, Inc. 306

Agency report date: August 5, 2026.

1. Compare your item

This notice names a product; your particular item is not yet verified. Compare every applicable model, serial, lot, production-date or model-year boundary below.

Product named: Pack Angiography NCMC 3/Cs BANNER
Company / brand: Medical Action Industries
Lot / serial / date codes: UDI-DI: 20809160490416. Lot/Expiration: 342513(1/16/2028), 336758(9/20/2027), 338977(1/16/2028)
Distribution: US: AZ, CO

Agency product description and boundaries

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

Still to verify: match the label on your item with the full official notice, including any exclusions, tables and photos. Some identifiers appear only on the agency website and are absent from this data feed. A missing field does not mean all versions are affected.

If your lot or date falls outside a stated range, this notice has not established that your item is affected. This is not a finding about other recalls or product safety.

2. Agency hazard and consumer action

FDA reports: 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.

No consumer remedy instructions are supplied in this record. Check the official notice and listed company contact for the agency’s current instructions.

Class I: most serious — reasonable probability of serious health consequences or death.

Affected product: Pack Angiography NCMC 3/Cs BANNER

3. Open the official notice or contact

View the official FDA enforcement record (openFDA) ↗

Official recall ID: Z-2792-2026
Brand: Medical Action Industries
Classification: Class I
Units affected: 657
Recall status: Ongoing
Initiated: Voluntary: Firm initiated

Affected products

Pack Angiography NCMC 3/Cs BANNER

Companies & origin

Recalling firm location: Arden, NC, United States
Firm address: 25 Heywood Rd, N/A, 28704-9302

Identifying details (verbatim from the notice)

Product codes / lots: UDI-DI: 20809160490416. Lot/Expiration: 342513(1/16/2028), 336758(9/20/2027), 338977(1/16/2028)
Distribution: US: AZ, CO
Firm notified the public via: N/A
FDA event ID: 99337
Recall initiated: May 13, 2026
FDA classified: July 30, 2026
FDA report date: August 5, 2026

Verify with the official sources:

CPSC — consumer products ↗ (aggregated here)
NHTSA — vehicles, car seats, tires ↗ (aggregated here; use NHTSA's VIN lookup to check a specific vehicle)
FDA — food, drugs, medical devices ↗ (aggregated here)
USDA FSIS — meat, poultry & processed egg products ↗ (not aggregated here)
Recalls.gov — the U.S. government’s all-agency portal ↗

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Source: U.S. Food & Drug Administration. Agency excerpts come from the public data feed and may omit tables or later changes; the linked government source is authoritative. Source last checked September 7, 2026 at 6:00 AM UTC. Record retrieved September 7, 2026 at 6:00 AM UTC.

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