---
title: "Pack Angiography NCMC 3/Cs BANNER, REF: NCAG62I, containing Medline Namic Ang... — FDA record Z-2792-2026 | Is It on Recall"
description: "Cardiovascular procedure kits contain manifolds, the subject of another recall, that may have particulate within the fluid path, which has the potential to be i"
url: https://isitonrecall.com/recall/fda-device-z-2792-2026-pack-angiography-ncmc-3-cs-banner-ref-ncag62i-containing-medline-namic-angiographic-star-off-handle/
updated: 2026-10-01
site: "Is It on Recall"
language: en
---

[Recall archive](https://isitonrecall.com/archives/) / FDA device enforcement

# Pack Angiography NCMC 3/Cs BANNER, REF: NCAG62I, containing Medline Namic Angiographic Star Off Handle Manifolds — FDA record Z-2792-2026

Reported ongoing

Status as reported in the agency record. FDA warns that enforcement status may not track the current recall lifecycle; check the current official notice.

Source date May 13, 2026. Retrieved Oct 1, 2026. Last updated Oct 1, 2026.

Archive changed Oct 1, 2026. USDA FSIS records are unavailable; [check FSIS directly](https://www.fsis.usda.gov/recalls). [Source coverage and dates](https://isitonrecall.com/sources/).

## What the record says

- **Product**: Pack Angiography NCMC 3/Cs BANNER, REF: NCAG62I, containing Medline Namic Angiographic Star Off Handle Manifolds
- **Reason**: 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.
- **Classification**: Class I
- **Recalling firm**: Medical Action Industries, Inc. 306
- **Quantity**: 657
- **Agency-reported status**: Ongoing
- **Source record identifier**: Z-2792-2026

[Open the official record](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-2792-2026%22)

[What the recall classes mean](https://isitonrecall.com/guides/recall-classes/). Classification is an agency assessment, not individual medical advice.

## Lot and product identifiers

| Label field | Details supplied by the agency |
| --- | --- |
| Lot, code or applicability | UDI-DI: 20809160490416. Lot/Expiration: 342513(1/16/2028), 336758(9/20/2027), 338977(1/16/2028) |

Match all identifying details in the current notice. A brand name alone is not enough.

## Distribution

US: AZ, CO

States below are derived from the distribution text, including nationwide wording. They are not inferred from the firm's address.

- [Arizona](https://isitonrecall.com/state/arizona/)
- [Colorado](https://isitonrecall.com/state/colorado/)

## Dates in the source

- **Report date**: Aug 5, 2026
- **Recall initiation date**: May 13, 2026
- **Center classification date**: Jul 30, 2026

FDA company pages use the listing date; enforcement records use initiation dates; CPSC uses recall date; NHTSA uses report-received date. These dates are not interchangeable.

## What to do next

Read the official notice for the action that applies to your exact product.

[Read the current instructions](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-2792-2026%22)

## Related records

[Medical devices records](https://isitonrecall.com/category/medical-devices/) [Medical Action Industries, Inc. 306 records](https://isitonrecall.com/brand/medical-action-industries-inc-306/)