Arrow International Inc: Medical Device Recall in 2018 - (Recall #: Z-0649-2018)

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:

Pressure Injectable ARROWg+ard Blue PLUS MultiLumen Central Venous Catheterization Kit; Product Codes: ASK-45703-PNHS; ASK-45703-PGMCL; ASK-45703-PNW; Exp. Dates Feb 2018 - Nov 2018

Product Classification:

Class II

Date Initiated: October 17, 2017

Date Posted: February 28, 2018

Recall Number: Z-0649-2018

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 Code ASK-45703-PNHS: 23F16M0498 Product Code ASK-45703-PGMCL: 23F17A0505 Product Code ASK-45703-PNW: 23F17B0116

Distribution Pattern:

Distribution US Nationwide

Voluntary or Mandated:

Voluntary: Firm initiated