Arrow International Inc: Medical Device Recall in 2015 - (Recall #: Z-1082-2015)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2015.

Data Source: FDA.

Product Description:

ARROWg+ard Blue PLUS Pressure Injectable Two-Lumen CVC Kit. The Multiple-Lumen Catheter permits venous access to the central circulation by way of the femoral jugular, or subclavian veins.

Product Classification:

Class II

Date Initiated: January 2, 2015

Date Posted: February 18, 2015

Recall Number: Z-1082-2015

Event ID: 70175

Reason for Recall:

Foreign material found within the kits. The foreign material, white or black particles and/or thread, is visible and can beidentified by the user.

Status: Terminated

Product Quantity: 1195

Code Information:

product number CDC-42802-P1A, lot number 23F14A0063

Distribution Pattern:

Nationwide

Voluntary or Mandated:

Voluntary: Firm initiated