Arrow International Inc: Medical Device Recall in 2017 - (Recall #: Z-2328-2017)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2017.

Data Source: FDA.

Product Description:

Single-Lumen Central Venous Catheterization Kit with Blue FlexTip(R) Catheter, Catheter, Percutaneous The Arrow Single-Lumen Catheter permits venous access to the central circulation

Product Classification:

Class II

Date Initiated: May 9, 2017

Date Posted: June 21, 2017

Recall Number: Z-2328-2017

Event ID: 77232

Reason for Recall:

Arrow International is recalling the affected product because the packaging may not be completely sealed, which may compromise sterility.

Status: Terminated

Product Quantity: 27,485 units distributed in U.S., 4,371 units distributed internationally

Code Information:

Material number: Ask-04301-WBH Device Listing D040650

Distribution Pattern:

Worldwide Distribution - US (nationwide) and Canada

Voluntary or Mandated:

Voluntary: Firm initiated