Cook Incorporated recalls Beacon Tip 5.0 Fr Angiographic catheters are designed to facilitate diagnostic and therapeutic procedures. Catheters are

Recalled June 25, 2025 · FDA recall Z-1902-2025 · Cook Incorporated

Hazard

Cook Medical identified that catheters supplied in the affected device lots may experience tip separation. · FDA Class I

Units

26986 units

Sold at

Worldwide distribution.

Description

Cook Medical identified that catheters supplied in the affected device lots may experience tip separation.

Product

Beacon Tip 5.0 Fr Angiographic catheters are designed to facilitate diagnostic and therapeutic procedures. Catheters are available in various configurations. Configurations include different shaft lengths and tip curves and some catheters are manufactured with a hydrophilic coating. Refer to the product label for product specifications (e.g., catheter length, distal curve configuration).

Manufacturer(s)

Cook Incorporated

Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →