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FDA (Device enforcement)Recalled 2026-03-11class ii

ARROW INTERNATIONAL, LLC: 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)2

Hazard

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

Details from the source

Reason for recall: Due to receiving a notice from a supplier that the liquid adhesive was incorrectly manufactured Distribution: U.S. Nationwide distribution in the states of AZ, CA, GA, MA, ME, MI, OR, PA, and VA. Quantity: 675 Lot/code info: Product code:ASK-04220-UCL1 UDI code: (01)10801902159127(17)270331(11)251203(10)33F25J0352 Batch Number: 33F25J0352 Product code: ASK-04020-EUH2 UDI code: (01)10801902213379(17)270731(11)251218(10)33F25J0869 Batch Number: 33F25J0869 Product code: ASK-04020-FMC UDI code: (01)10801902212099(17)270731(11)251218(10)33F25J0870 Batch Number: 33F25J0870 Product code: ASK-04020-MMC UDI code: (01)10801902117769(17)271130(11)251211(10)33F25J0880 Batch Number: 33F25J0880

UPC codes

10801902159127, 10801902213379, 10801902212099, 10801902117769

Source

Official record: FDA (Device enforcement)

Republished from the official source above; details can change — the source record controls.

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