Arrow International Inc: Medical Device Recall in 2018 - (Recall #: Z-0655-2018)

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:

AGB+ Multi Lumen Central Venous Catheterization Kit; Product Codes: CDC-42703-XP1A and CDC-47702-XP1A; Exp. Dates Feb 2018 - Nov 2018

Product Classification:

Class II

Date Initiated: October 17, 2017

Date Posted: February 28, 2018

Recall Number: Z-0655-2018

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 numbers: Product Codes CDC-42703-XP1A: 23F16M0507 Product Code CDC-47702-XP1A: 23F17A0533

Distribution Pattern:

Distribution US Nationwide

Voluntary or Mandated:

Voluntary: Firm initiated