Z-1166-2018 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

ARROWg+ard Blue PLUS Pressure Injectable Multi-Lumen CVC Kit. Intended to permit venous access to the 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

CDC-42703-P1A CDC-45703-P1A 13F16H0215 13F16H0216 13F16J0157 13F16J0053 13F16J0182 13F16J0186 13F16K0119 13F16K0266