FDAFDA recall Z-2792-2026 · Aug 5, 2026
Medical Action Industries, Inc. 306: Pack Angiography NCMC 3/Cs BANNER recall
Recall found
Product
Pack Angiography NCMC 3/Cs BANNER, REF: NCAG62I, containing Medline Namic Angiographic Star Off Handle Manifolds
Reason for recall
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.
What to do
FDA enforcement reports don't include consumer instructions. Check the codes below against your packaging. If this is a medicine or device you use, talk to your pharmacist or doctor before you stop or change anything, and contact the company or FDA for what to do with the product.
Recall details
- FDA classification
- Class I: FDA's most serious class, where use of or exposure to the product may cause serious health problems or death.
- Status
- Ongoing
- Codes, lots and dates
- UDI-DI: 20809160490416. Lot/Expiration: 342513(1/16/2028), 336758(9/20/2027), 338977(1/16/2028)
- Quantity
- 657
- Distribution
- US: AZ, CO
- Recalling firm
- Medical Action Industries, Inc. 306, Arden, NC
- Voluntary or mandated
- Voluntary: Firm initiated
- Recall started
- 2026-05-13
Source: openFDA enforcement record Z-2792-2026 · search recall number Z-2792-2026 in FDA's Enforcement Report.
Copied from the agency record without changes. Data as of Oct 22, 2026, 4:56 AM EDT. The agency notice is the final word.