Z-1163-2018 Class II Terminated

Recalled by Arrow International Inc — Reading, PA

Recall Details

Product Type
Devices
Report Date
March 28, 2018
Initiation Date
November 14, 2017
Termination Date
July 15, 2019
Voluntary/Mandated
Voluntary: Firm initiated
Product Quantity
18,124 total

Product Description

Pressure Injectable Multi- Lumen Central Venous Catheterization Kit with Blue FlexTip, ARROWg+ard Blue PLUS Catheter, Sharps Safety Features and Maximal Barrier Precautions. Permits venous access to central circulation.

Reason for Recall

Products do not contain the Central Venous Catheter Placement Procedures Note or the Central Line Insertion Checklist, which is a tool intended to guide clinicians in the use of best practices during central line insertions.

Distribution Pattern

Nationwide Distribution

Code Information

ASK-45703-PUR1 23F16H0385