Cap, Device Disinfectant

What Is It?

Disinfect needleless access valves and may act as a physical barrier to contamination if not removed for a set period of time

What Is FDA Product Code QBP?

Cap, Device Disinfectant is FDA product code QBP, Class 2, 21 CFR 880.5440.

What Does It Take to Sell It in the United States?

A 510(k) premarket notification is required before it is sold in the United States: the applicant shows the device is substantially equivalent to one already on the market. No clearance under this code names a Chinese applicant. A registration is not a clearance: the plants above are set up to make it, and the 510(k) it is sold under is held by whoever files it, often the brand.

What Do the Recalls Say?

The FDA has recorded 2 recalls under this product code since 2025. None was by a company in China. The root cause the FDA records most often is Process control (2).

A recall is a fact about one product and its maker, not a grade for every manufacturer of the type.