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ARROW INTERNATIONAL, LLC recalls Arrow Echogenic Introducer Needle REF ASK-04001-BWK2 UDI code: (01)10801902220315(17)261231(11)251210(10)33F25J0347
Recalled April 29, 2026 · FDA recall Z-1910-2026 · ARROW INTERNATIONAL
Hazard
Due to receiving a notice from a supplier that the liquid adhesive were incorrectly manufactured · FDA Class II
Units
85
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 were incorrectly manufactured
Product
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.
Manufacturer(s)
ARROW INTERNATIONAL, LLC
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →