Z-0653-2018 Class II Terminated

Recalled by Arrow International Inc — Reading, PA

Recall Details

Product Type
Devices
Report Date
February 28, 2018
Initiation Date
October 17, 2017
Termination Date
April 14, 2020
Voluntary/Mandated
Voluntary: Firm initiated
Product Quantity
5,926 total

Product Description

Pressure Injectable ARROWg+ard Blue PLUS Multi Lumen Central Venous Catheterization Kit; Product code: ASK-45703-PHF2; Exp. Dates Feb 2018 - Nov 2018

Reason for Recall

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

Distribution Pattern

Distribution US Nationwide

Code Information

Lot number: 23F17D0182