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

ARROW INTERNATIONAL, LLC: ARROW, ARROWG+ARD AND ARROWG+ARD BLUE PLUS PRESSURE INJECTABLE CENTRAL VENOUS CATHETER REF ASK-42802-PLH UDI code: (01)10801902133110(17)261231(11)251211(10)33F25L0140 REF AS

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: 395 Lot/code info: Product Code: ASK-42802-PLH UDI code: (01)10801902133110(17)261231(11)251211(10)33F25L0140 Batch Number: 33F25L0140 Product Code: ASK-45703-MGH UDI code: (01)10801902223675(17)261231(11)251209(10)33F25L0143 Batch Number: 33F25L0143 Product Code: ASK-42854-MGH UDI code: (01)10801902223668(17)261231(11)251210(10)33F25L0144 Batch Number: 33F25L0144 Product Code: ASK-45854-MGH UDI code: (01)10801902223699(17)261231(11)251209(10)33F25L0145 Batch Number: 33F25L0145

UPC codes

10801902133110, 10801902223675, 10801902223668, 10801902223699

Source

Official record: FDA (Device enforcement)

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

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