Arrow International Inc: Medical Device Recall in 2012 - (Recall #: Z-1823-2012)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2012.

Data Source: FDA.

Product Description:

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.

Product Classification:

Class II

Date Initiated: June 7, 2012

Date Posted: June 27, 2012

Recall Number: Z-1823-2012

Event ID: 62125

Reason for Recall:

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

Status: Terminated

Product Quantity: 1,085

Code Information:

Lot number RF2033361

Distribution Pattern:

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.

Voluntary or Mandated:

Voluntary: Firm initiated