FDA Enforcement Class II Terminated

Pressure Injectable ARROWg+ard Blue PLUS Multi Lumen Central Venous Catheterization Kit; Product Code: ASK 42703 PUHC; Exp. Dates Feb 2018 - Nov 2018

Recall: Z-0647-2018 · Reported February 28, 2018

Enforcement

Recall Number
Z-0647-2018
Event ID
79197
Classification
Class II
Status
Terminated
Product Type
Devices
Firm
Arrow International Inc
Voluntary / Mandated
Voluntary: Firm initiated
Initial Notification
Letter
Report Date
February 28, 2018
Initiation Date
October 17, 2017
Classification Date
February 20, 2018
Termination Date
April 14, 2020
Address
2400 Bernville Rd, N/A, Reading, PA, 19605-9607, United States

Description

Pressure Injectable ARROWg+ard Blue PLUS Multi Lumen Central Venous Catheterization Kit; Product Code: ASK 42703 PUHC; Exp. Dates Feb 2018 - Nov 2018

Reason

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

Code Info

Lot number: 23F16M0054

Distribution

Distribution US Nationwide

Quantity

5,926 total