Arrow International Inc recalls Arrow International, Inc. 7FR 3-Lumen Arrowg+ard Blue Plus(R) Pressure Injectable Central Venous Catheter - Catalog numb

Recalled June 27, 2012 · FDA recall Z-1823-2012 · Arrow International

Hazard

Arrow is recalling the product due to the possibility of voids in the catheter hub which could lead to an interlumen crossover. · FDA Class II

Units

1,085

Sold at

USA (nationwide) AL, AZ, AR, CA, CO, FL, GA, IL, IN, KS, LA, MA, MI, MO, NV, NH, NC, OH, PA, TX, VA, WA, and WI.

Description

Arrow is recalling the product due to the possibility of voids in the catheter hub which could lead to an interlumen crossover.

Product

Arrow International, Inc. 7FR 3-Lumen Arrowg+ard Blue Plus(R) Pressure Injectable Central Venous Catheter - Catalog number CDC-42703-XP1A The multiple-lumen pressure injectable catheter permits venous access to central circulation and injection of contrast media. The ARROWg+ard(R) antimicrobial surface is intended to provide protection against catheter-related infections.

Manufacturer(s)

Arrow International Inc

Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →