ARROW INTERNATIONAL, LLC recalls ARROW RADIAL ARTERY CATHETERIZATION KIT REF ASK-04220-UCL1 UDI code: (01)10801902159127(17)270331(11)251203(10)33F25J

Recalled April 29, 2026 · FDA recall Z-1911-2026 · ARROW INTERNATIONAL

Hazard

Due to receiving a notice from a supplier that the liquid adhesive was incorrectly manufactured · FDA Class II

Units

675

Sold at

U.S. Nationwide distribution in the states of AZ, CA, GA, MA, ME, MI, OR, PA, and VA.

Description

Due to receiving a notice from a supplier that the liquid adhesive was incorrectly manufactured

Product

ARROW RADIAL ARTERY CATHETERIZATION KIT REF ASK-04220-UCL1 UDI code: (01)10801902159127(17)270331(11)251203(10)33F25J0352 REF ASK-04020-EUH2 UDI code: (01)10801902213379(17)270731(11)251218(10)33F25J0869 REF ASK-04020-FMC UDI code: (01)10801902212099(17)270731(11)251218(10)33F25J0870 REF ASK-04020-MMC UDI code: (01)10801902117769(17)271130(11)251211(10)33F25J0880 The Arrow Arterial Catheterization Device permits access to the peripheral arterial circulation or to other small vessels.

Manufacturer(s)

ARROW INTERNATIONAL, LLC

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