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ARROW INTERNATIONAL, LLC recalls Pressure Injectable Arrowg+ard Blue Plus¿ Four-Lumen CVC Kit REF ASK-45854-PUPM1 UDI code: (01)10801902159578(17)270531
Recalled April 29, 2026 · FDA recall Z-1915-2026 · ARROW INTERNATIONAL
Hazard
Due to receiving a notice from a supplier that the liquid adhesive was incorrectly manufactured · FDA Class II
Units
5
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 was incorrectly manufactured
Product
Pressure Injectable Arrowg+ard Blue Plus¿ Four-Lumen CVC Kit REF ASK-45854-PUPM1 UDI code: (01)10801902159578(17)270531(11)251205(10)33F25M0011 The Arrowg+ard technology is intended to provide protection against catheter-related bloodstream infections (CRBSIs). It is not intended to be used as a treatment for existing infections nor is it indicated for long-term use (> 30 days). Clinical effectiveness of the Arrowg+ard Blue Plus catheter in preventing CRBSIs compared to the original Arrowg+ard Blue¿ catheter has not been studied
Manufacturer(s)
ARROW INTERNATIONAL, LLC
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →