FDAMarch 11, 2026device

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 ASK-45703-MGH UDI code: (01)10801902223675(17)261231(11)251209(10)33F25L0143 REF ASK-42854-MGH UDI code: (01)10801902223668(1...

Official recall recorded by the U.S. Food & Drug Administration.

The hazard

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

What to do

FDA enforcement status: Ongoing

Brands named

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UPCs

10801902133110108019022236751080190222366810801902223699

Recall history

Other federal recalls tied to the same brand — a factual pattern, straight from the source data.

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