FDAMarch 11, 2026device

Arrow Echogenic Introducer Needle REF ASK-04001-BWK2 UDI code: (01)10801902220315(17)261231(11)251210(10)33F25J0347 This device is intended for injection or aspiration of fluids. The needle protection device covers the needle after use to help prevent needle sticks.

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

The hazard

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

What to do

FDA enforcement status: Ongoing

Brands named

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UPCs

10801902220315

Recall history

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

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