Critical Alert
Medical Action Industries Recalls Pack Angiography NCMC 3/Cs BANNER
This is a Class I recall — the most serious type. There is a reasonable probability of serious health consequences or death.
Source: FDA
CriticalRecall #Z-2792-2026Medical Device
Medical Action Industries Recalls Pack Angiography NCMC 3/Cs BANNER
Medical Action Industries, Inc. 306 · Class I — Most Serious
Product Description
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.
FDA Classification
Class I — Most Serious
A situation in which there is a reasonable probability that the use of, or exposure to, a violative product will cause serious adverse health consequences or death.
Distribution
US: AZ, CO
Remedy
Consumers should stop using this product. Contact the recalling firm for further instructions regarding this product.
411 Press Analysis
Medical Action Industries, Inc. 306 is recalling a medical device classified as Class I by the FDA — the highest risk level. The recall was initiated on May 13, 2026 affecting 657. 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. It was distributed in US: AZ, CO. Consumers and healthcare professionals should exercise caution and discontinue use of the recalled product. Contact the recalling firm directly for return or disposal instructions.
Sources: FDA openFDA Enforcement Database
This recall appears in: Drug & Medical Product Contamination.