Arrow International Inc: Medical Device Recall in 2018 - (Recall #: Z-0650-2018)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2018.

Data Source: FDA.

Product Description:

Multi Lumen Central Venous Catheterization Kit; Product Code: ASK-12703-HH2; Exp. Dates Feb 2018 - Nov 2018

Product Classification:

Class II

Date Initiated: October 17, 2017

Date Posted: February 28, 2018

Recall Number: Z-0650-2018

Event ID: 79197

Reason for Recall:

These finished good kits may contain the incorrect Springwire Guide (SWG).

Status: Terminated

Product Quantity: 5,926 total

Code Information:

Lot number: 23F17C0652

Distribution Pattern:

Distribution US Nationwide

Voluntary or Mandated:

Voluntary: Firm initiated